A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15674359



Internal ID6794529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39681158..39683253hg38UCSC Ensembl
Innerchr17:39681202..39683210hg38UCSC Ensembl
Outerchr17:39681115..39683297hg38UCSC Ensembl
chr17:37837411..37839506hg19UCSC Ensembl
Innerchr17:37837455..37839463hg19UCSC Ensembl
Outerchr17:37837368..37839550hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382096
hg192096
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640547
Supporting Variants
SamplesNA20887
Known GenesPGAP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15674359
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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