A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702473



Internal ID15439125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124470928..124531906hg38UCSC Ensembl
Innerchr9:127233207..127294185hg19UCSC Ensembl
Innerchr9:126273028..126334006hg18UCSC Ensembl
Innerchr9:124312761..124373739hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3860979
hg1960979
hg1860979
hg1760979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526209
Supporting Variants
Samples
Known GenesNR5A1, NR6A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702473
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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