A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767687



Internal ID20543547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168679091..168679091hg38UCSC Ensembl
chr6:169079612..169079612hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767687
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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