A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046698



Internal ID20613738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37971301..37973600hg38UCSC Ensembl
chr19:38461941..38464240hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531151
Supporting Variants
Samples
Known GenesSIPA1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046698
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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