A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031796



Internal ID19121018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:140828261..140894169hg38UCSC Ensembl
Innerchr8:141838360..141904268hg19UCSC Ensembl
Innerchr8:141907542..141973450hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3865909
hg1965909
hg1865909
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757501
Samples
Known GenesPTK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031796
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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