A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000931



Internal ID21910274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122875130..122875183hg38UCSC Ensembl
chr8:123887369..123887422hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578652
Samples
Known GenesZHX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000931
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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