A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520039



Internal ID15100646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121527783..121600223hg38UCSC Ensembl
Innerchr9:124290062..124362502hg19UCSC Ensembl
Innerchr9:123329883..123402323hg18UCSC Ensembl
Innerchr9:121369616..121442056hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3872441
hg1972441
hg1872441
hg1772441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686695, nssv660192, nssv702919, nssv682718
Samples
Known GenesDAB2IP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520039
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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