A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765858



Internal ID20541718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39694237..39694237hg38UCSC Ensembl
chr17:37850490..37850490hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275595
Samples
Known GenesERBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765858
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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