A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516671



Internal ID15443964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:70832442..70853888hg38UCSC Ensembl
Innerchr17:68828583..68850029hg19UCSC Ensembl
Innerchr17:66340178..66361624hg18UCSC Ensembl
Innerchr17:66340178..66361624hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3821447
hg1921447
hg1821447
hg1721447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685774, nssv670067, nssv662834, nssv654931
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516671
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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