A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016932



Internal ID21926275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76046299..76046353hg38UCSC Ensembl
chr7:75675617..75675671hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564612
Samples
Known GenesSTYXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016932
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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