A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv725008



Internal ID16018964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158520155..158541655hg38UCSC Ensembl
Innerchr1:158489945..158511445hg19UCSC Ensembl
Innerchr1:156756569..156778069hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3821501
hg1921501
hg1821501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547982
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)nssv725008
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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