A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427646



Internal ID22485516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146576691..146576792hg38UCSC Ensembl
chr3:146294478..146294579hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902012
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427646
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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