A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv713449



Internal ID15660719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:54627627..54628260hg38UCSC Ensembl
Innerchr1:55093300..55093933hg19UCSC Ensembl
Innerchr1:54865888..54866521hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38634
hg19634
hg18634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546280
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)nssv713449
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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