A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197787



Internal ID20764827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35800510..35803516hg38UCSC Ensembl
chr19:36291412..36294418hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg383007
hg193007
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526035
Supporting Variants
Samples
Known GenesPRODH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197787
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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