A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920857



Internal ID22696080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131632663..131632967hg38UCSC Ensembl
chr11:131502557..131502861hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366028
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920857
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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