A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900011



Internal ID22675148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179915030..179917297hg38UCSC Ensembl
chr5:179342030..179344297hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg382268
hg192268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900011
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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