A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10917552



Internal ID6704691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8968388..8979795hg38UCSC Ensembl
Innerchr3:8968397..8979786hg38UCSC Ensembl
Outerchr3:8968379..8979804hg38UCSC Ensembl
chr3:9010072..9021479hg19UCSC Ensembl
Innerchr3:9010081..9021470hg19UCSC Ensembl
Outerchr3:9010063..9021488hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3811408
hg1911408
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595231
Supporting Variants
SamplesNA20828
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10917552
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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