A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917242



Internal ID22692461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81357742..81404996hg38UCSC Ensembl
chr11:81068785..81116038hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3847255
hg1947254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917242
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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