A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046692



Internal ID20613732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37937815..37951629hg38UCSC Ensembl
chr19:38428455..38442269hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg3813815
hg1913815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523909
Supporting Variants
Samples
Known GenesSIPA1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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