A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708608



Internal ID15655878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1663759..1706566hg38UCSC Ensembl
Innerchr1:1595198..1638005hg19UCSC Ensembl
Innerchr1:1585061..1627865hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3842808
hg1942808
hg1842805
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545020
Supporting Variants
Samples
Known GenesCDK11A, CDK11B, MMP23A, SLC35E2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708608
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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