A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529030



Internal ID8423305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40664273..40720497hg38UCSC Ensembl
Innerchr15:40956471..41012695hg19UCSC Ensembl
Innerchr15:38743763..38799987hg18UCSC Ensembl
Innerchr15:38743763..38799987hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3856225
hg1956225
hg1856225
hg1756225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705741
Samples
Known GenesRAD51, RAD51-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529030
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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