A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv739987



Internal ID15687257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248586905..248638700hg38UCSC Ensembl
Innerchr1:248750206..248802001hg19UCSC Ensembl
Innerchr1:246816829..246868624hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3851796
hg1951796
hg1851796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549693
Supporting Variants
Samples
Known GenesOR2T10, OR2T11, OR2T35
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv739987
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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