A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545006



Internal ID16332415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1452075..1496418hg38UCSC Ensembl
Innerchr1:1387455..1431798hg19UCSC Ensembl
Innerchr1:1377318..1421661hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3844344
hg1944344
hg1844344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv34n54
Supporting Variantsnssv708591
Samples
Known GenesATAD3B, ATAD3C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545006
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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