A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548054



Internal ID15988777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:159926189..159937651hg38UCSC Ensembl
Innerchr1:159895979..159907441hg19UCSC Ensembl
Innerchr1:158162603..158174065hg18UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3811463
hg1911463
hg1811463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv727672
Samples
Known GenesIGSF9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548054
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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