A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661864



Internal ID15051830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69486486..69504046hg38UCSC Ensembl
Innerchr9:72101402..72118962hg19UCSC Ensembl
Innerchr9:71291222..71308782hg18UCSC Ensembl
Innerchr9:69330956..69348516hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3817561
hg1917561
hg1817561
hg1717561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515519
Supporting Variants
Samples
Known GenesAPBA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661864
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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