A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074952



Internal ID21984185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136239752..136239752hg38UCSC Ensembl
chr6:136560890..136560890hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576519
Samples
Known GenesMTFR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074952
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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