A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199676



Internal ID20766716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56349501..56390000hg38UCSC Ensembl
chr19:56860870..56901369hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3840500
hg1940500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528794
Supporting Variants
Samples
Known GenesZNF542, ZNF582
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199676
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00021


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