A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018280



Internal ID21927623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67273145..67355298hg38UCSC Ensembl
chr7:66738132..66820285hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3882154
hg1982154
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573873
Samples
Known GenesLOC101929736, PMS2P4, STAG3L4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018280
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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