A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545614



Internal ID21869969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51694006..51694096hg38UCSC Ensembl
chr3:51728022..51728112hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5994133
Supporting Variants
Samples
Known GenesTEX264
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545614
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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