A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630036



Internal ID21822083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10826816..10826816hg38UCSC Ensembl
chr17:10730133..10730133hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088164
Supporting Variants
Samples
Known GenesPIRT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630036
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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