A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019538



Internal ID19108756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:50159790..50201129hg38UCSC Ensembl
Innerchr5:49455624..49496963hg19UCSC Ensembl
Innerchr5:49491381..49532720hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3841340
hg1941340
hg1841340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642036, nssv3642037, nssv3642035
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)nsv1019538
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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