A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639884



Internal ID7026662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8353768..8356705hg38UCSC Ensembl
Innerchr17:8353782..8356691hg38UCSC Ensembl
Outerchr17:8353754..8356719hg38UCSC Ensembl
chr17:8257086..8260023hg19UCSC Ensembl
Innerchr17:8257100..8260009hg19UCSC Ensembl
Outerchr17:8257072..8260037hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382938
hg192938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15606857
SamplesHG03684
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639884
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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