A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928975



Internal ID22704221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88062986..88126515hg38UCSC Ensembl
chr16:88096592..88160121hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3863530
hg1963530
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373256
Samples
Known GenesBANP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928975
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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