A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619053



Internal ID21811100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18179597..18201088hg38UCSC Ensembl
chr19:18290407..18311898hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3821492
hg1921492
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040871
Supporting Variants
Samples
Known GenesMPV17L2, RAB3A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619053
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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