A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv739675



Internal ID15686945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:247698214..247723700hg38UCSC Ensembl
Innerchr1:247861516..247887002hg19UCSC Ensembl
Innerchr1:245928139..245953625hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3825487
hg1925487
hg1825487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549598
Supporting Variants
Samples
Known GenesOR6F1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv739675
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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