A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141447



Internal ID21440543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81886660..81887001hg38UCSC Ensembl
chr5:81182479..81182820hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568050
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141447
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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