A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637432



Internal ID21829479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17594030..17600643hg38UCSC Ensembl
chr17:17497344..17503957hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg386614
hg196614
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028124
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637432
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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