A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045231



Internal ID20612271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2260041..2261127hg38UCSC Ensembl
chr19:2260040..2261126hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381087
hg191087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529963
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045231
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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