A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391064



Internal ID22448934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132878790..132879886hg38UCSC Ensembl
chr3:132597634..132598730hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381097
hg191097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905414
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17391064
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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