A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244808



Internal ID21303954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111573634..111575348hg38UCSC Ensembl
Outerchr5:111565528..111581474hg38UCSC Ensembl
Innerchr5:110909331..110911045hg19UCSC Ensembl
Outerchr5:110901226..110917171hg19UCSC Ensembl
Innerchr5:110937230..110938944hg18UCSC Ensembl
Outerchr5:110929125..110945070hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3815947
hg1915946
hg1815946
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169418
Supporting Variants
SamplesNGO_1
Known GenesSTARD4-AS1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244808
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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