A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744712



Internal ID20520714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80401620..80403988hg38UCSC Ensembl
chr17:78375420..78377788hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382369
hg192369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283338
Samples
Known GenesLOC100294362
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744712
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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