A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921231



Internal ID22696454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119501302..119506903hg38UCSC Ensembl
chr11:119372013..119377614hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385602
hg195602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364502
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921231
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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