A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400863



Internal ID22458733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126316205..126316462hg38UCSC Ensembl
chr3:126035048..126035305hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894295
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400863
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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