A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077867



Internal ID21987100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144781055..144781055hg38UCSC Ensembl
chr7:144478148..144478148hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558795
Samples
Known GenesTPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077867
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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