A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087857



Internal ID21277724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:125213637..125265754hg38UCSC Ensembl
Innerchr6:125534783..125586900hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3852118
hg1952118
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112886
Supporting Variants
Samplessample256
Known GenesTPD52L1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087857
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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