A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569577



Internal ID16010300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:56790808..56933568hg38UCSC Ensembl
Innerchr15:57083006..57225766hg19UCSC Ensembl
Innerchr15:54870298..55013058hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38142761
hg19142761
hg18142761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149221
SamplesHGDP01023
Known GenesLOC145783, TCF12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569577
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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