A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049480



Internal ID20616520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57656969..57657214hg38UCSC Ensembl
chr19:58168337..58168582hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529580
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049480
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00125


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