A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122394



Internal ID21403224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179524534..179524656hg38UCSC Ensembl
chr5:178951535..178951657hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572366
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122394
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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