A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640212



Internal ID7026987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20753268..20779479hg38UCSC Ensembl
Innerchr17:20753268..20779479hg38UCSC Ensembl
Outerchr17:20752768..20779979hg38UCSC Ensembl
chr17:20656581..20682792hg19UCSC Ensembl
Innerchr17:20656581..20682792hg19UCSC Ensembl
Outerchr17:20656081..20683292hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3826212
hg1926212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15649013, essv15649014
SamplesNA19467, HG03072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640212
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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