A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741435



Internal ID20517412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98140078..98140137hg38UCSC Ensembl
chr7:97769390..97769449hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274748
Samples
Known GenesLMTK2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741435
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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