A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075099



Internal ID21984332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164093513..164093513hg38UCSC Ensembl
chr6:164514545..164514545hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559915
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075099
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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