A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682089



Internal ID15072055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102955808..103236914hg38UCSC Ensembl
Innerchr9:105718090..105999196hg19UCSC Ensembl
Innerchr9:104757911..105039017hg18UCSC Ensembl
Innerchr9:102797645..103078751hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38281107
hg19281107
hg18281107
hg17281107
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516844
Supporting Variants
Samples
Known GenesCYLC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682089
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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