A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629502



Internal ID21821549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21096307..21102785hg38UCSC Ensembl
chr17:20999620..21006098hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg386479
hg196479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033977
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629502
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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