A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569246



Internal ID16356655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43599314..43688523hg38UCSC Ensembl
Innerchr15:43891512..43980721hg19UCSC Ensembl
Innerchr15:41678804..41768013hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3889210
hg1989210
hg1889210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4501n54
Supporting Variantsnssv842239
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)nsv569246
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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