A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13910216



Internal ID2936261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98283647..98287879hg38UCSC Ensembl
Innerchr10:98283662..98287865hg38UCSC Ensembl
Outerchr10:98283633..98287894hg38UCSC Ensembl
chr10:100043404..100047636hg19UCSC Ensembl
Innerchr10:100043419..100047622hg19UCSC Ensembl
Outerchr10:100043390..100047651hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg384233
hg194233
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624333
Supporting Variants
SamplesHG02595
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13910216
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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