A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062273



Internal ID19151492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24196288..24304880hg38UCSC Ensembl
Innerchr19:24379090..24487682hg19UCSC Ensembl
Innerchr19:24170930..24279522hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38108593
hg19108593
hg18108593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3485n100
Supporting Variantsnssv3570678
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)nsv1062273
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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