A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417896



Internal ID22475766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79221049..79222723hg38UCSC Ensembl
chr5:78516872..78518546hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381675
hg191675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897661
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417896
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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