A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526942



Internal ID15454235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8986913..8990996hg38UCSC Ensembl
Innerchr19:9097589..9101672hg19UCSC Ensembl
Innerchr19:8958589..8962672hg18UCSC Ensembl
Innerchr19:8958589..8962672hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384084
hg194084
hg184084
hg174084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv198n21
Supporting Variantsnssv703311
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526942
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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