A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660192



Internal ID15050158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121527783..121582159hg38UCSC Ensembl
Innerchr9:124290062..124344438hg19UCSC Ensembl
Innerchr9:123329883..123384259hg18UCSC Ensembl
Innerchr9:121369616..121423992hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3854377
hg1954377
hg1854377
hg1754377
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520039
Supporting Variants
Samples
Known GenesDAB2IP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660192
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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