A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570111



Internal ID16357520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76994352..77040265hg38UCSC Ensembl
Innerchr15:77286693..77332606hg19UCSC Ensembl
Innerchr15:75073748..75119661hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3845914
hg1945914
hg1845914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv846206
Samples
Known GenesPSTPIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570111
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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