A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526166



Internal ID21850524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10902601..10902694hg38UCSC Ensembl
chr2:11042727..11042820hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5985535
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526166
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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