A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568922



Internal ID16356331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:33883771..33902385hg38UCSC Ensembl
Innerchr15:34175972..34194586hg19UCSC Ensembl
Innerchr15:31963264..31981878hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3818615
hg1918615
hg1818615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839800, nssv839799
Samples
Known GenesAVEN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568922
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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