A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280235



Internal ID20489453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79014076..79014076hg38UCSC Ensembl
chr6:79723793..79723793hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755230
Supporting Variants
Samples
Known GenesPHIP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280235
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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