A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276568



Internal ID20485786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10101062..10101062hg38UCSC Ensembl
chr2:10241189..10241189hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750521
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276568
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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