A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086636



Internal ID21281719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:86474047..86475468hg38UCSC Ensembl
Innerchr7:86103363..86104784hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg381422
hg191422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117940
Supporting Variants
Samplessample316
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086636
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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