A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078919



Internal ID21988152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88992136..88992136hg38UCSC Ensembl
chr6:89701855..89701855hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078919
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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