A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv725009



Internal ID16018965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158550415..158587049hg38UCSC Ensembl
Innerchr1:158520205..158556839hg19UCSC Ensembl
Innerchr1:156786829..156823463hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3836635
hg1936635
hg1836635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547986
Supporting Variants
Samples
Known GenesOR10X1, OR6P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv725009
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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