A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925491



Internal ID22700718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10326743..10327567hg38UCSC Ensembl
chr11:10348290..10349114hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38825
hg19825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368903
Samples
Known GenesCAND1.11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925491
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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