A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17581821



Internal ID21773864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4827318..4827502hg38UCSC Ensembl
chr10:4869510..4869694hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011431
Supporting Variants
Samples
Known GenesAKR1E2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17581821
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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