A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006363



Internal ID21915706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157611693..157611807hg38UCSC Ensembl
chr7:157404385..157404499hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563089
Samples
Known GenesPTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006363
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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