A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136043



Internal ID21450202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23434029..23438333hg38UCSC Ensembl
chr3:23475520..23479824hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384305
hg194305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571534
Supporting Variants
SamplesHG01114
Known GenesMIR548AC, UBE2E2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136043
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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