A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421077



Internal ID22478947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8113798..8114063hg38UCSC Ensembl
chr3:8155485..8155750hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890500
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421077
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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