A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622238



Internal ID7009097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5861771..5864739hg38UCSC Ensembl
Innerchr10:5861788..5864722hg38UCSC Ensembl
Outerchr10:5861754..5864756hg38UCSC Ensembl
chr10:5903734..5906702hg19UCSC Ensembl
Innerchr10:5903751..5906685hg19UCSC Ensembl
Outerchr10:5903717..5906719hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382969
hg192969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13687150, essv13687152, essv13687155, essv13687149, essv13687151, essv13687153, essv13687154
SamplesNA19222, HG03133, NA19904, NA18868, HG02477, NA19913, HG03159
Known GenesANKRD16
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622238
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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