A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198417



Internal ID20765457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20386915..21526140hg38UCSC Ensembl
chr19:20497724..21708942hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381139226
hg191211219
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528948
Supporting Variants
Samples
Known GenesLINC00664, MIR1270-1, MIR1270-2, ZNF429, ZNF430, ZNF431, ZNF493, ZNF626, ZNF708, ZNF714, ZNF737, ZNF738, ZNF826P, ZNF85
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198417
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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