A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879974



Internal ID22654944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74766849..74771948hg38UCSC Ensembl
chr16:74800747..74805846hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473363, nssv17479650
Samples
Known GenesFA2H
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879974
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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