A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425001



Internal ID22482871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188045964..188050792hg38UCSC Ensembl
chr3:187763752..187768580hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg384829
hg194829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903239
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425001
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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