A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790678



Internal ID21236016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60982124..60982124hg38UCSC Ensembl
chr11:60749596..60749596hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13690657, nssv13677092
Samples
Known GenesCD6
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790678
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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