A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568598



Internal ID16009321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:26082319..26575978hg38UCSC Ensembl
Innerchr15:26327466..26821125hg19UCSC Ensembl
Innerchr15:23878559..24372218hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38493660
hg19493660
hg18493660
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839149
Samples
Known GenesGABRB3, LINC00929
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568598
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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