A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv842234



Internal ID15789504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43599314..43646090hg38UCSC Ensembl
Innerchr15:43891512..43938288hg19UCSC Ensembl
Innerchr15:41678804..41725580hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3846777
hg1946777
hg1846777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569243
Supporting Variants
Samples
Known GenesCATSPER2, CKMT1B, RNU6-28P, STRC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv842234
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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