A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104622



Internal ID21269395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:156340590..156343976hg38UCSC Ensembl
Innerchr2:157197102..157200488hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg383387
hg193387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111381
Supporting Variants
Samplessample138
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104622
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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