A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061731



Internal ID21970964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77545307..77545307hg38UCSC Ensembl
chr6:78255024..78255024hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg385950
hg195950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568690
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061731
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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