A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002061



Internal ID21911404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158330185..158342603hg38UCSC Ensembl
chr7:158122877..158135295hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3812419
hg1912419
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568951
Samples
Known GenesPTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002061
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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