A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529089



Internal ID21853446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15611834..15611914hg38UCSC Ensembl
chr2:15751958..15752038hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5986469
Supporting Variants
Samples
Known GenesDDX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529089
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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