A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028988



Internal ID19118207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120071670..120106440hg38UCSC Ensembl
Innerchr5:119407365..119442135hg19UCSC Ensembl
Innerchr5:119435264..119470034hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3834771
hg1934771
hg1834771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647980
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028988
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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