A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418986



Internal ID22476856
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 StatusS
Merged Variantsnsv5900011
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418986
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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