A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415601



Internal ID22473471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44510750..44510799hg38UCSC Ensembl
chr3:44552242..44552291hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889426
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415601
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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