A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14082772



Internal ID21288633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:156449170..156452911hg38UCSC Ensembl
Innerchr5:155876180..155879921hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg383742
hg193742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117622
Supporting Variants
Samplessample419
Known GenesSGCD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14082772
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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