A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105704



Internal ID21274924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:85887209..85889292hg38UCSC Ensembl
Innerchr2:86114332..86116415hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg382084
hg192084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115855
Supporting Variants
Samplessample214
Known GenesST3GAL5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105704
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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