A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066986



Internal ID18809517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29967456..30014480hg38UCSC Ensembl
Innerchr19:30458363..30505387hg19UCSC Ensembl
Innerchr19:35150203..35197227hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3847025
hg1947025
hg1847025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3510n100
Supporting Variantsnssv3566559
Samples
Known GenesURI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066986
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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