A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282205



Internal ID20491423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62143082..62143082hg38UCSC Ensembl
chr11:61910554..61910554hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755791
Supporting Variants
Samples
Known GenesINCENP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282205
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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