A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061452



Internal ID18803983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7657750..7785131hg38UCSC Ensembl
Innerchr19:7722636..7850017hg19UCSC Ensembl
Innerchr19:7628636..7756017hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38127382
hg19127382
hg18127382
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564672
Samples
Known GenesC19orf59, CD209, CLEC4G, CLEC4M, FCER2, RETN, TRAPPC5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061452
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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