A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275595



Internal ID20484813
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 StatusS
Merged Variantsnsv4765858
Supporting Variants
Samples
Known GenesERBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275595
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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