A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046260



Internal ID20613300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34912643..34917474hg38UCSC Ensembl
chr19:35403547..35408378hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384832
hg194832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529638
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046260
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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