A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14084296



Internal ID21269998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:132148743..132151056hg38UCSC Ensembl
Innerchr7:131833502..131835815hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg382314
hg192314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111207
Supporting Variants
Samplessample146
Known GenesPLXNA4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14084296
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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