A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17627987



Internal ID21820034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67951495..67951495hg38UCSC Ensembl
chr17:65947611..65947611hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095857
Supporting Variants
Samples
Known GenesBPTF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17627987
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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