A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046151



Internal ID20613191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:28953477..28960835hg38UCSC Ensembl
chr19:29444384..29451742hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg387359
hg197359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517281
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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