A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv713447



Internal ID15660717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:54627522..54629333hg38UCSC Ensembl
Innerchr1:55093195..55095006hg19UCSC Ensembl
Innerchr1:54865783..54867594hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381812
hg191812
hg181812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546278
Supporting Variants
Samples
Known GenesACOT11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv713447
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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