A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139555



Internal ID21462123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148929639..148930092hg38UCSC Ensembl
chr3:148647426..148647879hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38454
hg19454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567475
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139555
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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