A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741104



Internal ID20517081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72554017..72554083hg38UCSC Ensembl
chr17:70550157..70550223hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272510
Samples
Known GenesLINC00673
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741104
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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