A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065094



Internal ID21974327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138737115..138737115hg38UCSC Ensembl
chr7:138421860..138421860hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572546
Samples
Known GenesATP6V0A4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065094
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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