A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059622



Internal ID19148841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27419755hg38UCSC Ensembl
Innerchr19:27747981..27910663hg19UCSC Ensembl
Innerchr19:32439821..32602503hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38162683
hg19162683
hg18162683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3495n100
Supporting Variantsnssv3570824
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059622
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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