A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080947



Internal ID21990180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71565837..71565837hg38UCSC Ensembl
chr11:71276883..71276883hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592553
Samples
Known GenesKRTAP5-10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080947
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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