A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199681



Internal ID20766721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56512518..56705265hg38UCSC Ensembl
chr19:57023887..57216633hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38192748
hg19192747
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531530
Supporting Variants
Samples
Known GenesSMIM17, ZFP28, ZNF470, ZNF471, ZNF71, ZNF835
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199681
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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