A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621929



Internal ID21813976
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 StatusS
Merged Variantsnsv6025226
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621929
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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