A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624205



Internal ID7011061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91344809..91350318hg38UCSC Ensembl
Innerchr10:91344847..91350281hg38UCSC Ensembl
Outerchr10:91344772..91350356hg38UCSC Ensembl
chr10:93104566..93110075hg19UCSC Ensembl
Innerchr10:93104604..93110038hg19UCSC Ensembl
Outerchr10:93104529..93110113hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg385510
hg195510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13894407, essv13894406, essv13894412, essv13894411, essv13894409, essv13894405, essv13894410, essv13894404, essv13894408, essv13894413
SamplesHG01485, HG01624, NA20774, HG00185, HG00313, HG01360, NA19658, HG01055, HG01378, NA11832
Known GenesLOC100188947
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624205
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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