A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569247



Internal ID16009970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43601620..43647444hg38UCSC Ensembl
Innerchr15:43893818..43939642hg19UCSC Ensembl
Innerchr15:41681110..41726934hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3845825
hg1945825
hg1845825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842240
Samples
Known GenesCATSPER2, RNU6-28P, STRC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569247
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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