A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024426



Internal ID19113643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:60086917..60097975hg38UCSC Ensembl
Innerchr8:60999476..61010534hg19UCSC Ensembl
Innerchr8:61162030..61173088hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3811059
hg1911059
hg1811059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7234n100
Supporting Variantsnssv3689467
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)nsv1024426
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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