A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112659



Internal ID21295925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:43611849..43616491hg38UCSC Ensembl
Innerchr7:43651448..43656090hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg384643
hg194643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084860, nssv14084226
Samplessample50, sample136
Known GenesSTK17A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112659
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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