A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200179



Internal ID20767219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53396844..53470433hg38UCSC Ensembl
chr19:53900097..53973687hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3873590
hg1973591
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531696
Supporting Variants
Samples
Known GenesTPM3P9, ZNF761, ZNF765, ZNF813
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200179
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00026


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