A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15757191



Internal ID22091667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60982123..60982123hg38UCSC Ensembl
chr11:60749595..60749595hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4446181
Supporting Variants
Samples
Known GenesCD6
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15757191
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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