A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619084



Internal ID21811131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46134388..46240987hg38UCSC Ensembl
chr19:46637645..46744244hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38106600
hg19106600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057747
Supporting Variants
Samples
Known GenesDKFZp434J0226, IGFL1, IGFL2, RNU6-66P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619084
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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