A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419107



Internal ID22476977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:130742560..130912125hg38UCSC Ensembl
chr5:130078253..130247818hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg38169566
hg19169566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419107
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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