A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565753



Internal ID21757718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:72089841..72089841hg38UCSC Ensembl
chr6:72799544..72799544hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6074861
Supporting Variants
Samples
Known GenesRIMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565753
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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