A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646918



Internal ID7033660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34158043..34160541hg38UCSC Ensembl
Innerchr21:34158086..34160499hg38UCSC Ensembl
Outerchr21:34158001..34160584hg38UCSC Ensembl
chr21:35530343..35532841hg19UCSC Ensembl
Innerchr21:35530386..35532799hg19UCSC Ensembl
Outerchr21:35530301..35532884hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg382499
hg192499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16313683, essv16313695, essv16313712, essv16313727, essv16313742, essv16313707, essv16313740, essv16313724, essv16313691, essv16313700, essv16313698, essv16313682, essv16313735, essv16313696, essv16313745, essv16313701, essv16313684, essv16313722, essv16313749, essv16313710, essv16313738, essv16313703, essv16313723, essv16313730, essv16313708, essv16313739, essv16313718, essv16313704, essv16313690, essv16313753, essv16313717, essv16313754, essv16313688, essv16313692, essv16313697, essv16313719, essv16313709, essv16313686, essv16313731, essv16313699, essv16313751, essv16313750, essv16313693, essv16313716, essv16313743, essv16313713, essv16313748, essv16313741, essv16313736, essv16313747, essv16313689, essv16313681, essv16313732, essv16313746, essv16313733, essv16313680, essv16313755, essv16313720, essv16313687, essv16313744, essv16313752, essv16313725, essv16313706, essv16313702, essv16313726, essv16313721, essv16313734, essv16313715, essv16313711, essv16313714, essv16313694, essv16313729, essv16313728, essv16313685, essv16313705, essv16313737
SamplesHG02574, HG03548, HG03052, NA19204, NA18861, HG03517, HG02836, HG03115, HG03280, NA20346, HG03139, NA19190, NA20356, HG03478, HG03464, HG01325, HG02541, NA20317, HG02549, HG03079, HG02981, NA19317, NA19189, NA18864, HG03073, HG03055, NA19451, HG03088, HG02582, NA18933, HG03547, NA19327, HG02322, NA18516, HG03457, HG03428, HG02953, HG03575, NA18910, HG03124, HG03294, HG03382, HG02577, NA19042, HG03078, NA19338, NA19257, NA19095, HG01107, NA19149, NA19434, NA19144, NA19439, NA20281, HG03419, HG02558, HG03103, HG02771, HG03565, HG03432, HG03049, HG02938, NA19474, NA19093, HG03063, HG02462, NA20289, HG03351, HG03401, NA19121, HG03445, HG02947, NA19146, NA19463, HG02643, NA19429
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646918
Frequency
Sample Size2504
Observed Gain0
Observed Loss76
Observed Complex0
Frequencyn/a


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