A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545009



Internal ID16332418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1452888..1504314hg38UCSC Ensembl
Innerchr1:1388268..1439694hg19UCSC Ensembl
Innerchr1:1378131..1429557hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3851427
hg1951427
hg1851427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv34n54
Supporting Variantsnssv708595
Samples
Known GenesATAD3B, ATAD3C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545009
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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