A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197785



Internal ID20764825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3571861..3588811hg38UCSC Ensembl
chr19:3571859..3588809hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3816951
hg1916951
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528754
Supporting Variants
Samples
Known GenesGIPC3, HMG20B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197785
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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