A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066579



Internal ID21975812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121935495..121935495hg38UCSC Ensembl
chr7:121575549..121575549hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563580
Samples
Known GenesPTPRZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066579
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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