A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085007



Internal ID21287473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122919737..122922263hg38UCSC Ensembl
Innerchr7:122559791..122562317hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg382527
hg192527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112800
Supporting Variants
Samplessample402
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085007
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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