A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066709



Internal ID18809240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:90898..293934hg38UCSC Ensembl
Innerchr19:90898..293934hg19UCSC Ensembl
Innerchr19:41898..244934hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38203037
hg19203037
hg18203037
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3419n100
Supporting Variantsnssv3564592
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)nsv1066709
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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