A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524612



Internal ID15105219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101786434..101826646hg38UCSC Ensembl
Innerchr15:102326637..102366849hg19UCSC Ensembl
Innerchr15:100144160..100184372hg18UCSC Ensembl
Innerchr15:100144160..100184372hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3840213
hg1940213
hg1840213
hg1740213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700573
Samples
Known GenesOR4F15, OR4F6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524612
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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