A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv739776



Internal ID15687046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248568548..248616640hg38UCSC Ensembl
Innerchr1:248731849..248779941hg19UCSC Ensembl
Innerchr1:246798472..246846564hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3848093
hg1948093
hg1848093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549646
Supporting Variants
Samples
Known GenesOR2T10, OR2T34
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv739776
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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