A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525591



Internal ID15452884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125985901..126038145hg38UCSC Ensembl
Innerchr9:128748180..128800424hg19UCSC Ensembl
Innerchr9:127788001..127840245hg18UCSC Ensembl
Innerchr9:125827734..125879978hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3852245
hg1952245
hg1852245
hg1752245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701733
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525591
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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