A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075943



Internal ID21985176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10307875..10307875hg38UCSC Ensembl
chr6:10308108..10308108hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075943
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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