A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082057



Internal ID21991290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73377583..73377583hg38UCSC Ensembl
chr10:75137341..75137341hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581443
Samples
Known GenesANXA7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082057
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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