A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610754



Internal ID16051477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:19561983..19667783hg38UCSC Ensembl
Innerchr8:19419494..19525294hg19UCSC Ensembl
Innerchr8:19463774..19569574hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38105801
hg19105801
hg18105801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1107466
Samples
Known GenesCSGALNACT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610754
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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