A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123792



Internal ID21483574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145381459..145407528hg38UCSC Ensembl
chr5:144761022..144787091hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3826070
hg1926070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569774
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123792
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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