A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031439



Internal ID19120661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136669376..136832890hg38UCSC Ensembl
Innerchr8:137681619..137845133hg19UCSC Ensembl
Innerchr8:137750801..137914315hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38163515
hg19163515
hg18163515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3692731
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)nsv1031439
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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