A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145644



Internal ID21447597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87073922..87074011hg38UCSC Ensembl
chr5:86369739..86369828hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584217
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145644
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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