A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199680



Internal ID20766720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56476001..56479200hg38UCSC Ensembl
chr19:56987370..56990569hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527229
Supporting Variants
Samples
Known GenesZNF667, ZNF667-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199680
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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