A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731372



Internal ID20507292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40811149..40811209hg38UCSC Ensembl
chr17:38967401..38967461hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268375
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731372
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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