A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv725263



Internal ID15672533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158757357..158761117hg38UCSC Ensembl
Innerchr1:158727147..158730907hg19UCSC Ensembl
Innerchr1:156993771..156997531hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg383761
hg193761
hg183761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548016
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv725263
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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