A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031776



Internal ID19120998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2473547..2716218hg38UCSC Ensembl
Innerchr8:2330755..2573751hg19UCSC Ensembl
Innerchr8:2318162..2561158hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38242672
hg19242997
hg18242997
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6820n100
Supporting Variantsnssv3675243
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)nsv1031776
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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