A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935357



Internal ID22710697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36793433..37314449hg38UCSC Ensembl
chr19:37284335..37805351hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38521017
hg19521017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408278
Samples
Known GenesLOC284412, ZNF345, ZNF383, ZNF420, ZNF568, ZNF585A, ZNF585B, ZNF790, ZNF790-AS1, ZNF829
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935357
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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