A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527720



Internal ID15455013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104529720..104531740hg38UCSC Ensembl
Innerchr9:107292001..107294021hg19UCSC Ensembl
Innerchr9:106331822..106333842hg18UCSC Ensembl
Innerchr9:104371556..104373576hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg382021
hg192021
hg182021
hg172021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv492n21
Supporting Variantsnssv704201
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527720
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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