A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13894254



Internal ID3006200
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624194
Supporting Variants
SamplesHG02651
Known GenesHTR7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13894254
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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