A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943836



Internal ID22719291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18962443..19048413hg38UCSC Ensembl
chr13:19536583..19622553hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3885971
hg1985971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373898
Samples
Known GenesLINC00442
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943836
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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