A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527234



Internal ID8421509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40695527..40739488hg38UCSC Ensembl
Innerchr15:40987725..41031686hg19UCSC Ensembl
Innerchr15:38775017..38818978hg18UCSC Ensembl
Innerchr15:38775017..38818978hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3843962
hg1943962
hg1843962
hg1743962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703634
Samples
Known GenesRAD51, RMDN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527234
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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