A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525901



Internal ID15453194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22945120..22949247hg38UCSC Ensembl
Innerchr9:22945119..22949246hg19UCSC Ensembl
Innerchr9:22935119..22939246hg18UCSC Ensembl
Innerchr9:22935119..22939246hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg384128
hg194128
hg184128
hg174128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702105
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525901
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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