A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890816



Internal ID22665845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179849614..179849913hg38UCSC Ensembl
chr5:179276614..179276913hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419770
Samples
Known GenesC5orf45
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890816
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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