A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047863



Internal ID20614903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39198699..39201487hg38UCSC Ensembl
chr19:39689339..39692127hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382789
hg192789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528813
Supporting Variants
Samples
Known GenesNCCRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047863
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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