A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063744



Internal ID18806275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14906349..14999775hg38UCSC Ensembl
Innerchr19:15017161..15110587hg19UCSC Ensembl
Innerchr19:14878161..14971587hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3893427
hg1993427
hg1893427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564780
Samples
Known GenesOR7C2, SLC1A6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063744
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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