A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133407



Internal ID21466239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81014531..81014973hg38UCSC Ensembl
chr3:81063682..81064124hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574326
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133407
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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