A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287903



Internal ID20497121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216560026..216560026hg38UCSC Ensembl
chr2:217424749..217424749hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754475
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287903
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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