A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001431



Internal ID21910774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122815982..122816046hg38UCSC Ensembl
chr8:123828221..123828285hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582654
Samples
Known GenesZHX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001431
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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