A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568916



Internal ID16356325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32676722..32731750hg38UCSC Ensembl
Innerchr15:32968923..33023951hg19UCSC Ensembl
Innerchr15:30756215..30811243hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3855029
hg1955029
hg1855029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839794
Samples
Known GenesGREM1, LOC100131315, SCG5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568916
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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