A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049195



Internal ID20616235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55516347..55523967hg38UCSC Ensembl
chr19:56027714..56035334hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg387621
hg197621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519708
Supporting Variants
Samples
Known GenesSSC5D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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