A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875275



Internal ID22650233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1880215..1883714hg38UCSC Ensembl
chr16:1930216..1933715hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469832, nssv17469831
Samples
Known GenesLINC00254
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875275
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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