A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926770



Internal ID22701997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54733072..54778789hg38UCSC Ensembl
chr11:51340491..51386208hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3845718
hg1945718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363735
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926770
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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