A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879333



Internal ID22654302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74670413..74672212hg38UCSC Ensembl
chr16:74704311..74706110hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479121, nssv17473361
Samples
Known GenesMLKL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879333
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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