A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916026



Internal ID22691245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123060985..123061120hg38UCSC Ensembl
chr11:122931693..122931828hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357202
Samples
Known GenesHSPA8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916026
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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