A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117622



Internal ID21300888
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 StatusM
Merged Variants
Supporting Variantsnssv14082772
Samplessample419
Known GenesSGCD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117622
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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