A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199712



Internal ID20766752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57620355..57646335hg38UCSC Ensembl
chr19:58131723..58157703hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3825981
hg1925981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532213
Supporting Variants
Samples
Known GenesZNF134, ZNF211
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199712
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00051


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer