A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086738



Internal ID21283397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16309399..16362465hg38UCSC Ensembl
Innerchr7:16349024..16402090hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3853067
hg1953067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117070
Supporting Variants
Samplessample343
Known GenesISPD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086738
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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