A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562397



Internal ID21886752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73485348..73485348hg38UCSC Ensembl
chr6:74195071..74195071hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065210
Supporting Variants
Samples
Known GenesMTO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562397
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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