A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199730



Internal ID20766770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57990019..57990578hg38UCSC Ensembl
chr19:58501387..58501946hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528156
Supporting Variants
Samples
Known GenesZNF606
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199730
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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