A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569244



Internal ID16356653
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842236, nssv842237, nssv842235
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)nsv569244
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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