A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523391



Internal ID15450684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:38371566..38396870hg38UCSC Ensembl
Innerchr15:38663767..38689071hg19UCSC Ensembl
Innerchr15:36451059..36476363hg18UCSC Ensembl
Innerchr15:36451059..36476363hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3825305
hg1925305
hg1825305
hg1725305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699141
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523391
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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