A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067349



Internal ID21976582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90494379..90494379hg38UCSC Ensembl
chr6:91204098..91204098hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38968
hg19968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067349
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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