A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024641



Internal ID18767173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:115694413..115787777hg38UCSC Ensembl
Innerchr5:115030110..115123474hg19UCSC Ensembl
Innerchr5:115058009..115151373hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3893365
hg1993365
hg1893365
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5788n100
Supporting Variantsnssv3647085
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)nsv1024641
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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