A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700677



Internal ID15437329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101966623..101984851hg38UCSC Ensembl
Innerchr9:104728905..104747133hg19UCSC Ensembl
Innerchr9:103768726..103786954hg18UCSC Ensembl
Innerchr9:101808460..101826688hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3818229
hg1918229
hg1818229
hg1718229
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521116
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700677
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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