A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576190



Internal ID21768233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35271333..35271395hg38UCSC Ensembl
chr8:35128851..35128913hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003357
Supporting Variants
Samples
Known GenesUNC5D
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576190
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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