A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843582



Internal ID15790852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59563027..59664354hg38UCSC Ensembl
Innerchr15:59855226..59956553hg19UCSC Ensembl
Innerchr15:57642518..57743845hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38101328
hg19101328
hg18101328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569605
Supporting Variants
Samples
Known GenesBNIP2, GCNT3, GTF2A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843582
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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