A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073620



Internal ID21982853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13794540..13794540hg38UCSC Ensembl
chr6:13794772..13794772hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569922
Samples
Known GenesMCUR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073620
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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