A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937030



Internal ID22712392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52519523..52847521hg38UCSC Ensembl
chr19:53022776..53350774hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38327999
hg19327999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407360
Samples
Known GenesZNF137P, ZNF28, ZNF468, ZNF600, ZNF611, ZNF701, ZNF808, ZNF83
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937030
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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