A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582017



Internal ID21774060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:141252654..141252901hg38UCSC Ensembl
chr8:142262753..142263000hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006331
Supporting Variants
Samples
Known GenesSLC45A4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582017
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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