A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018672



Internal ID21928015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149878469..149878554hg38UCSC Ensembl
chr7:149575558..149575643hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558349
Samples
Known GenesATP6V0E2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018672
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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