A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv739989



Internal ID15687259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248586905..248645922hg38UCSC Ensembl
Innerchr1:248750206..248809223hg19UCSC Ensembl
Innerchr1:246816829..246875846hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3859018
hg1959018
hg1859018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549694
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)nssv739989
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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