A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569665



Internal ID16357074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62413995..62424486hg38UCSC Ensembl
Innerchr15:62706194..62716685hg19UCSC Ensembl
Innerchr15:60493486..60503977hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3810492
hg1910492
hg1810492
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4567n54
Supporting Variantsnssv843832
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569665
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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