A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531809



Internal ID21856165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38756187..38756306hg38UCSC Ensembl
chr2:38983329..38983448hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989257
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531809
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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