A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624194



Internal ID7011050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90811285..90811865hg38UCSC Ensembl
Innerchr10:90811335..90811815hg38UCSC Ensembl
Outerchr10:90811203..90811947hg38UCSC Ensembl
chr10:92571042..92571622hg19UCSC Ensembl
Innerchr10:92571092..92571572hg19UCSC Ensembl
Outerchr10:92570960..92571704hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13894255, essv13894251, essv13894262, essv13894249, essv13894253, essv13894259, essv13894256, essv13894252, essv13894258, essv13894260, essv13894261, essv13894254, essv13894257, essv13894250
SamplesNA19684, NA18988, HG00188, HG00183, NA20862, NA12234, NA20525, HG00140, HG02651, NA20852, HG00131, NA19726, NA11843, HG01507
Known GenesHTR7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624194
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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