A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520727



Internal ID21845086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:156369029..156369222hg38UCSC Ensembl
chr2:157225541..157225734hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5986533
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520727
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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