A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721139



Internal ID144805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8336853..8390896hg38UCSC Ensembl
chr19:8401737..8455780hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3854044
hg1954044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523972
Supporting Variants
Samples
Known GenesANGPTL4, KANK3, MIR4999, RAB11B, RAB11B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721139
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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