A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125075



Internal ID21512005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113024276..113032474hg38UCSC Ensembl
chr3:112743123..112751321hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg388199
hg198199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581017
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125075
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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