A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044485



Internal ID20611525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16351081..16354812hg38UCSC Ensembl
chr19:16461892..16465623hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg383732
hg193732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044485
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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