A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528794



Internal ID20902155
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 StatusM
Merged Variants
Supporting Variantsnssv18199676
Samples
Known GenesZNF542, ZNF582
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528794
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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