A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527236



Internal ID15454529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73128898..73177194hg38UCSC Ensembl
Innerchr15:73421239..73469535hg19UCSC Ensembl
Innerchr15:71208292..71256588hg18UCSC Ensembl
Innerchr15:71208292..71256588hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3848297
hg1948297
hg1848297
hg1748297
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703636
Samples
Known GenesNEO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527236
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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