A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516235



Internal ID15443528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113637872..113644764hg38UCSC Ensembl
Innerchr9:116400152..116407044hg19UCSC Ensembl
Innerchr9:115439973..115446865hg18UCSC Ensembl
Innerchr9:113479706..113486598hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg386893
hg196893
hg186893
hg176893
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700402, nssv704684, nssv662941, nssv655392, nssv697365, nssv690027, nssv679572, nssv702472, nssv699610, nssv657125, nssv666982, nssv694760, nssv681493, nssv692791, nssv657928
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516235
Frequency
Sample Size2026
Observed Gain3
Observed Loss12
Observed Complex0
Frequencyn/a


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