A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1107465



Internal ID15613965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:19507372..19582466hg38UCSC Ensembl
Innerchr8:19364883..19439977hg19UCSC Ensembl
Innerchr8:19409163..19484257hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3875095
hg1975095
hg1875095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610753
Supporting Variants
Samples
Known GenesCSGALNACT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1107465
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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