A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525112



Internal ID15452405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32748367..32754687hg38UCSC Ensembl
Innerchr9:32748365..32754685hg19UCSC Ensembl
Innerchr9:32738365..32744685hg18UCSC Ensembl
Innerchr9:32738365..32744685hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg386321
hg196321
hg186321
hg176321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv484n21
Supporting Variantsnssv701174
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525112
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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