A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv851221



Internal ID15798491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101794654..101829508hg38UCSC Ensembl
Innerchr15:102334857..102369711hg19UCSC Ensembl
Innerchr15:100152380..100187234hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3834855
hg1934855
hg1834855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570915
Supporting Variants
Samples
Known GenesOR4F15, OR4F6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv851221
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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