A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515899



Internal ID15096506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112596769..112831590hg38UCSC Ensembl
Innerchr9:115359049..115593870hg19UCSC Ensembl
Innerchr9:114398870..114633691hg18UCSC Ensembl
Innerchr9:112438604..112673425hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38234822
hg19234822
hg18234822
hg17234822
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693083, nssv679688, nssv690694, nssv692622, nssv692354, nssv656683, nssv696532, nssv655701, nssv674489, nssv665191, nssv662159, nssv692817
Samples
Known GenesINIP, KIAA1958, SNX30
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515899
Frequency
Sample Size2026
Observed Gain11
Observed Loss1
Observed Complex0
Frequencyn/a


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