A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971338



Internal ID22746273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64948616..64948616hg38UCSC Ensembl
chr11:64716088..64716088hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354427
Samples
Known GenesC11orf85
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971338
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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