A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564780



Internal ID18516375
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 StatusS
Merged Variantsnsv1063744
Supporting Variants
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)nssv3564780
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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