A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708616



Internal ID15655886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1688102..1732685hg38UCSC Ensembl
Innerchr1:1619541..1664124hg19UCSC Ensembl
Innerchr1:1609404..1653984hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3844584
hg1944584
hg1844581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545027
Supporting Variants
Samples
Known GenesCDK11A, CDK11B, MMP23A, SLC35E2, SLC35E2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708616
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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