A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262562



Internal ID20471780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222951470..222951470hg38UCSC Ensembl
chr1:223124812..223124812hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756717
Supporting Variants
Samples
Known GenesDISP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262562
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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