A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421634



Internal ID22479504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109162813..109162942hg38UCSC Ensembl
chr5:108498514..108498643hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5904540
Supporting Variants
Samples
Known GenesFER
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421634
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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