A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv713473



Internal ID15660743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:54628151..54629245hg38UCSC Ensembl
Innerchr1:55093824..55094918hg19UCSC Ensembl
Innerchr1:54866412..54867506hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381095
hg191095
hg181095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546295
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)nssv713473
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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