A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521046



Internal ID15448339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91694432..91714136hg38UCSC Ensembl
Innerchr9:94456714..94476418hg19UCSC Ensembl
Innerchr9:93496535..93516239hg18UCSC Ensembl
Innerchr9:91536269..91555973hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3819705
hg1919705
hg1819705
hg1719705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv490n21
Supporting Variantsnssv697752
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521046
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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