A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063639



Internal ID18806170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:90898..283856hg38UCSC Ensembl
Innerchr19:90898..283856hg19UCSC Ensembl
Innerchr19:41898..234856hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38192959
hg19192959
hg18192959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3419n100
Supporting Variantsnssv3564591
Samples
Known GenesLINC01002, OR4F17, PPAP2C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063639
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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