A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929013



Internal ID22704260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45073984..45074322hg38UCSC Ensembl
chr19:45577242..45577580hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400042
Samples
Known GenesZNF296
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929013
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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