A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516724



Internal ID15444017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:79973311..79987809hg38UCSC Ensembl
Innerchr9:82588226..82602724hg19UCSC Ensembl
Innerchr9:81778046..81792544hg18UCSC Ensembl
Innerchr9:79817780..79832278hg17UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3814499
hg1914499
hg1814499
hg1714499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv670459, nssv691594
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516724
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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