A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705206



Internal ID15095172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:27771369..27772288hg38UCSC Ensembl
Innerchr8:27628886..27629805hg19UCSC Ensembl
Innerchr8:27684805..27685724hg18UCSC Ensembl
Innerchr8:27684805..27685724hg17UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38920
hg19920
hg18920
hg17920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528584
Supporting Variants
Samples
Known GenesCCDC25
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705206
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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