A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925765



Internal ID22700992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:23723857..23724165hg38UCSC Ensembl
chr11:23745403..23745711hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925765
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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