A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142543



Internal ID21413957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95851771..95851925hg38UCSC Ensembl
chr5:95187475..95187629hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583535
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142543
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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