A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085869



Internal ID21995102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75469289..75469289hg38UCSC Ensembl
chr10:77229047..77229047hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583906
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085869
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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