A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067489



Internal ID19156708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:5510216..5540392hg38UCSC Ensembl
Innerchr19:5510227..5540403hg19UCSC Ensembl
Innerchr19:5461227..5491403hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3830177
hg1930177
hg1830177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564610
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)nsv1067489
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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