A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516327



Internal ID15443620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78280693..78301191hg38UCSC Ensembl
Innerchr17:76276774..76297272hg19UCSC Ensembl
Innerchr17:73788369..73808867hg18UCSC Ensembl
Innerchr17:73788369..73808867hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3820499
hg1920499
hg1820499
hg1720499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv667596, nssv684100, nssv693335, nssv661385, nssv682263, nssv705809, nssv674977
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516327
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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