A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152967



Internal ID21509288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:92301776..92305032hg38UCSC Ensembl
chr5:91597593..91600849hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg383257
hg193257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580422
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152967
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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