A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031784



Internal ID19121006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:1570505..1648607hg38UCSC Ensembl
Innerchr8:1518671..1596773hg19UCSC Ensembl
Innerchr8:1506078..1584180hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3878103
hg1978103
hg1878103
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6803n100
Supporting Variantsnssv3675044
Samples
Known GenesDLGAP2, LOC100507435
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031784
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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