A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640696



Internal ID6680782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:47304736..47307029hg38UCSC Ensembl
Innerchr17:47304886..47306879hg38UCSC Ensembl
Outerchr17:47304586..47307179hg38UCSC Ensembl
chr17:45382102..45384395hg19UCSC Ensembl
Innerchr17:45382252..45384245hg19UCSC Ensembl
Outerchr17:45381952..45384545hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg382294
hg192294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15686262, essv15686263
SamplesHG02887, HG03378
Known GenesITGB3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640696
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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