A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645497



Internal ID7032246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21828229..21829227hg38UCSC Ensembl
Innerchr20:21828385..21829177hg38UCSC Ensembl
Outerchr20:21828141..21829315hg38UCSC Ensembl
chr20:21808867..21809865hg19UCSC Ensembl
Innerchr20:21809023..21809815hg19UCSC Ensembl
Outerchr20:21808779..21809953hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg38999
hg19999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16158091, essv16158086, essv16158079, essv16158090, essv16158087, essv16158080, essv16158077, essv16158081, essv16158088, essv16158089, essv16158083, essv16158092, essv16158094, essv16158085, essv16158095, essv16158082, essv16158093, essv16158084, essv16158078
SamplesHG03096, HG03100, HG03515, HG03246, HG03268, HG03195, HG01440, NA19175, NA20126, HG03294, HG03024, NA19206, NA18909, HG02010, NA20348, NA19102, HG02051, HG02947, NA18488
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645497
Frequency
Sample Size2504
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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