A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17564738



Internal ID21889093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85872686..85872686hg38UCSC Ensembl
chr6:86582404..86582404hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070086
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17564738
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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