A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020996



Internal ID19110214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:134052558..134081206hg38UCSC Ensembl
Innerchr8:135064801..135093449hg19UCSC Ensembl
Innerchr8:135133983..135162631hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3828649
hg1928649
hg1828649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7324n100
Supporting Variantsnssv3692716
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)nsv1020996
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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