A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025226



Internal ID21934569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5256709..5257922hg38UCSC Ensembl
chr17:5160004..5161217hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg381214
hg191214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621929
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025226
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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