A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279948



Internal ID20489166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9660413..9670709hg38UCSC Ensembl
chr2:9800542..9810838hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3810297
hg1910297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739562
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279948
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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