A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075874



Internal ID21985107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149803478..149803478hg38UCSC Ensembl
chr6:150124614..150124614hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568222
Samples
Known GenesPCMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075874
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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