A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124958



Internal ID21506172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131259429..131259490hg38UCSC Ensembl
chr5:130595122..130595183hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582554
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124958
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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