A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019363



Internal ID19108581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:141195805..141236451hg38UCSC Ensembl
Innerchr8:142205904..142246550hg19UCSC Ensembl
Innerchr8:142275086..142315732hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3840647
hg1940647
hg1840647
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690078, nssv3690077
Samples
Known GenesSLC45A4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019363
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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