A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914601



Internal ID22689818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32583926..32587007hg38UCSC Ensembl
chr11:32605472..32608553hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383082
hg193082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361012
Samples
Known GenesEIF3M
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914601
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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