A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155748



Internal ID21425781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77752521..77752856hg38UCSC Ensembl
chr5:77048345..77048680hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580645
Supporting Variants
SamplesHG00731
Known GenesTBCA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155748
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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