A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098443



Internal ID22007676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88736587..88736587hg38UCSC Ensembl
chr16:88802995..88802995hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622664
Samples
Known GenesLOC100289580, PIEZO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098443
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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