A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032046



Internal ID19121268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:50159790..50301693hg38UCSC Ensembl
Innerchr5:49455624..49597527hg19UCSC Ensembl
Innerchr5:49491381..49633284hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg38141904
hg19141904
hg18141904
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5663n100
Supporting Variantsnssv3642115
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)nsv1032046
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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