A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879000



Internal ID22653967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75546466..75571986hg38UCSC Ensembl
chr16:75580364..75605884hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3825521
hg1925521
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473395
Samples
Known GenesGABARAPL2, TMEM231
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879000
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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