A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv726507



Internal ID16020463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158898012..158912726hg38UCSC Ensembl
Innerchr1:158867802..158882516hg19UCSC Ensembl
Innerchr1:157134426..157149140hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3814715
hg1914715
hg1814715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548026
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)nssv726507
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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