A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618223



Internal ID21810270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17030456..17030456hg38UCSC Ensembl
chr17:16933770..16933770hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084350
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618223
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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