A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085725



Internal ID21994958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73591381..73591381hg38UCSC Ensembl
chr11:73302426..73302426hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595630
Samples
Known GenesFAM168A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085725
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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