A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156353



Internal ID15533904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:19576510..19598962hg38UCSC Ensembl
Innerchr8:19434021..19456473hg19UCSC Ensembl
Innerchr8:19478301..19500753hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3822453
hg1922453
hg1822453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610755
Supporting Variants
SamplesNINDS_230
Known GenesCSGALNACT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156353
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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