A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096856



Internal ID21290283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111571140..111575078hg38UCSC Ensembl
Innerchr5:110906837..110910775hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg383939
hg193939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111927
Supporting Variants
Samplessample58
Known GenesSTARD4-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096856
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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