A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023402



Internal ID18765935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:50159790..50412624hg38UCSC Ensembl
Innerchr5:49455624..49708458hg19UCSC Ensembl
Innerchr5:49491381..49744215hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg38252835
hg19252835
hg18252835
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5664n100
Supporting Variantsnssv3642118
Samples
Known GenesEMB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023402
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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