A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018567



Internal ID18761100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:97743416..97782434hg38UCSC Ensembl
Innerchr8:98755644..98794662hg19UCSC Ensembl
Innerchr8:98824820..98863838hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3839019
hg1939019
hg1839019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689739
Samples
Known GenesLAPTM4B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018567
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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