A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv842235



Internal ID16136191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43599314..43647444hg38UCSC Ensembl
Innerchr15:43891512..43939642hg19UCSC Ensembl
Innerchr15:41678804..41726934hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3848131
hg1948131
hg1848131
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569244
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)nssv842235
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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