A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516587



Internal ID15097194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:83611204..83640850hg38UCSC Ensembl
Innerchr9:86226119..86255765hg19UCSC Ensembl
Innerchr9:85415939..85445585hg18UCSC Ensembl
Innerchr9:83455673..83485319hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3829647
hg1929647
hg1829647
hg1729647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669398, nssv661508
Samples
Known GenesIDNK
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516587
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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