A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067664



Internal ID21976897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101006587..101006587hg38UCSC Ensembl
chr6:101454463..101454463hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg382707
hg192707
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067664
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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