A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528725



Internal ID15109332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42463357..42812208hg38UCSC Ensembl
Innerchr15:42755555..43104406hg19UCSC Ensembl
Innerchr15:40542847..40891698hg18UCSC Ensembl
Innerchr15:40542847..40891698hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38348852
hg19348852
hg18348852
hg17348852
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705380
Samples
Known GenesCDAN1, HAUS2, LRRC57, SNAP23, STARD9, TTBK2, ZNF106
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528725
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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