A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867361



Internal ID22642296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105072286..105096751hg38UCSC Ensembl
chr11:104943013..104967478hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3824466
hg1924466
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455036
Samples
Known GenesCARD17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867361
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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