A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129883



Internal ID21487609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179119681..179119876hg38UCSC Ensembl
chr3:178837469..178837664hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575191
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129883
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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