A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933571



Internal ID22708884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74767114..74771700hg38UCSC Ensembl
chr16:74801012..74805598hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg384587
hg194587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387387
Samples
Known GenesFA2H
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933571
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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