A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077136



Internal ID21986369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:128005705..128005705hg38UCSC Ensembl
chr6:128326850..128326850hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg384103
hg194103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564344
Samples
Known GenesPTPRK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077136
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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