A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019956



Internal ID18762491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:1474951..1514278hg38UCSC Ensembl
Innerchr8:1423117..1462444hg19UCSC Ensembl
Innerchr8:1410524..1449851hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3839328
hg1939328
hg1839328
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757770
Samples
Known GenesDLGAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019956
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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