A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565345



Internal ID21757891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2694524..2694524hg38UCSC Ensembl
chr6:2694758..2694758hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080212
Supporting Variants
Samples
Known GenesMYLK4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565345
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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