A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656977



Internal ID9923082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:549016..559022hg38UCSC Ensembl
Outerchr19:548645..559392hg38UCSC Ensembl
Innerchr19:549016..559022hg19UCSC Ensembl
Outerchr19:548645..559392hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810748
hg1910748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6391672, essv6187210, essv6443654, essv6126392, essv6209830, essv6403839, essv6490039, essv5991438, essv6178453, essv5717165, essv5562669, essv6257853, essv6285020, essv6564981, essv5810320, essv5547118, essv5587885, essv6483338, essv5813933, essv5979878, essv6090872, essv6003671, essv6359771, essv6449900, essv6317731, essv6078306, essv6486905, essv6402289, essv5648095, essv5421186, essv5467748, essv5514906, essv5654563, essv5731064, essv5783386, essv6170646, essv5671566, essv6562022
SamplesNA19466, NA19350, NA19359, NA19393, NA19443, NA19446, NA19448, NA19457, NA19372, NA19471, NA19456, NA19445, NA19451, NA19437, NA19462, NA19347, NA19455, NA19461, NA19453, NA19338, NA19452, NA19469, NA19436, NA19440, NA19434, NA19473, NA19435, NA19470, NA19311, NA19467, NA19438, NA19472, NA19468, NA19430, NA19312, NA19463, NA19429, NA19431
Known GenesGZMM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656977
Frequency
Sample Size1151
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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