A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020811



Internal ID19110029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18607196..18666701hg38UCSC Ensembl
Innerchr5:18607305..18666810hg19UCSC Ensembl
Innerchr5:18643062..18702567hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3859506
hg1959506
hg1859506
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5593n100
Supporting Variantsnssv3635876, nssv3635880, nssv3635879, nssv3635872, nssv3635874, nssv3635881, nssv3635870, nssv3635875, nssv3635884, nssv3635882, nssv3635878, nssv3635873, nssv3635883, nssv3635877, nssv3635871
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)nsv1020811
Frequency
Sample Size11257
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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