A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473395



Internal ID22531288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75546466..75571986hg38UCSC Ensembl
chr16:75580364..75605884hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3825521
hg1925521
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879000
Supporting Variants
Samples
Known GenesGABARAPL2, TMEM231
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473395
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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