A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570565



Internal ID16357974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:95481301..95502540hg38UCSC Ensembl
Innerchr15:96024530..96045769hg19UCSC Ensembl
Innerchr15:93825534..93846773hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3821240
hg1921240
hg1821240
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv849047
Samples
Known GenesLINC00924
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570565
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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