A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275616



Internal ID20484834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77140495..77140495hg38UCSC Ensembl
chr1:77606180..77606180hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755415
Supporting Variants
Samples
Known GenesPIGK
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275616
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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