A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629580



Internal ID21821627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5863064..5863064hg38UCSC Ensembl
chr17:5766384..5766384hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6086615
Supporting Variants
Samples
Known GenesLOC339166
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629580
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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