A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905795



Internal ID22680987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43665664..43824318hg38UCSC Ensembl
chr5:43665766..43824420hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38158655
hg19158655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410527
Samples
Known GenesNNT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905795
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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