A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934734



Internal ID22710065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44096878..44096928hg38UCSC Ensembl
chr19:44601031..44601081hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406856
Samples
Known GenesZNF224
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934734
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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