A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619116



Internal ID21811163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31597993..31597993hg38UCSC Ensembl
chr17:29925012..29925012hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100203
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619116
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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