A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015343



Internal ID19104560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131443328..131566810hg38UCSC Ensembl
Innerchr8:132455575..132579057hg19UCSC Ensembl
Innerchr8:132524757..132648239hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38123483
hg19123483
hg18123483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757375
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)nsv1015343
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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