A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620863



Internal ID21812910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30237151..30237151hg38UCSC Ensembl
chr17:28564169..28564169hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094821
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620863
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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