A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640381



Internal ID7027156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32385922..32396957hg38UCSC Ensembl
Innerchr17:32385922..32396957hg38UCSC Ensembl
Outerchr17:32385820..32397008hg38UCSC Ensembl
chr17:30712941..30723976hg19UCSC Ensembl
Innerchr17:30712941..30723976hg19UCSC Ensembl
Outerchr17:30712839..30724027hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3811036
hg1911036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15659294, essv15659295
SamplesHG03126, NA19467
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640381
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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