A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035100



Internal ID19124319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:100876850..100908496hg38UCSC Ensembl
Innerchr8:101889078..101920724hg19UCSC Ensembl
Innerchr8:101958254..101989900hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3831647
hg1931647
hg1831647
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7275n100
Supporting Variantsnssv3689745, nssv3689744
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)nsv1035100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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