A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523608



Internal ID15450901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88931941..88948119hg38UCSC Ensembl
Innerchr9:91546856..91563034hg19UCSC Ensembl
Innerchr9:90736676..90752854hg18UCSC Ensembl
Innerchr9:88776410..88792588hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3816179
hg1916179
hg1816179
hg1716179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699402
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523608
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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