A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119815



Internal ID21453452
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 Variantsnsv5584154
Supporting Variants
SamplesHG02011
Known GenesKIAA0141
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119815
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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