A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029640



Internal ID19118858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136669376..136838087hg38UCSC Ensembl
Innerchr8:137681619..137850330hg19UCSC Ensembl
Innerchr8:137750801..137919512hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38168712
hg19168712
hg18168712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3692732
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029640
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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