A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049407



Internal ID20616447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8026101..8029800hg38UCSC Ensembl
chr19:8090985..8094684hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532818
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049407
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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