A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548007



Internal ID15988730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158757235..158761117hg38UCSC Ensembl
Innerchr1:158727025..158730907hg19UCSC Ensembl
Innerchr1:156993649..156997531hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg383883
hg193883
hg183883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv596n54
Supporting Variantsnssv725203
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548007
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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