A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062639



Internal ID21971872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135970951..135970951hg38UCSC Ensembl
chr7:135655699..135655699hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562446
Samples
Known GenesLUZP6, MTPN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062639
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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