A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415957



Internal ID22473827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9621891..9624696hg38UCSC Ensembl
chr3:9663575..9666380hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg382806
hg192806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5904713
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415957
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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