A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894661



Internal ID22669736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176919460..176919562hg38UCSC Ensembl
chr5:176346461..176346563hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415263
Samples
Known GenesUIMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894661
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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