A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640434



Internal ID7027209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34883365..34886789hg38UCSC Ensembl
Innerchr17:34883365..34886789hg38UCSC Ensembl
Outerchr17:34883242..34886910hg38UCSC Ensembl
chr17:33210384..33213808hg19UCSC Ensembl
Innerchr17:33210384..33213808hg19UCSC Ensembl
Outerchr17:33210261..33213929hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383425
hg193425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15664340, essv15664341
SamplesHG02736, HG03352
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640434
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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