A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708629



Internal ID15655899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1713469..1740343hg38UCSC Ensembl
Innerchr1:1644908..1671782hg19UCSC Ensembl
Innerchr1:1634768..1661642hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3826875
hg1926875
hg1826875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545035
Supporting Variants
Samples
Known GenesCDK11A, CDK11B, SLC35E2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708629
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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