A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619017



Internal ID21811064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39694303..39694303hg38UCSC Ensembl
chr17:37850556..37850556hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6098274
Supporting Variants
Samples
Known GenesERBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619017
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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