A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155391



Internal ID21504264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96622858..96622858hg38UCSC Ensembl
chr5:95958562..95958562hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5638451
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155391
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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