A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418929



Internal ID22476799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141928813..141929040hg38UCSC Ensembl
chr5:141308378..141308605hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906801
Supporting Variants
Samples
Known GenesKIAA0141
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418929
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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