A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941296



Internal ID22716718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43796944..43797107hg38UCSC Ensembl
chr19:44301096..44301259hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390452
Samples
Known GenesLYPD5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941296
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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