A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295449



Internal ID20504667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6495929..6495929hg38UCSC Ensembl
chr2:6636061..6636061hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753255
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295449
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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