A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548025



Internal ID16335434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158898012..158909957hg38UCSC Ensembl
Innerchr1:158867802..158879747hg19UCSC Ensembl
Innerchr1:157134426..157146371hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3811946
hg1911946
hg1811946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv599n54
Supporting Variantsnssv726504
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548025
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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