A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286603



Internal ID20495821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107280050..107280050hg38UCSC Ensembl
chr6:107601254..107601254hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755569
Supporting Variants
Samples
Known GenesPDSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286603
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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