A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063107



Internal ID18805638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6890127..7108040hg38UCSC Ensembl
Innerchr19:6890138..7108051hg19UCSC Ensembl
Innerchr19:6841138..7059051hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38217914
hg19217914
hg18217914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3421n100
Supporting Variantsnssv3723271, nssv3564639, nssv3564640, nssv3564643, nssv3723270, nssv3723268, nssv3564642, nssv3723269, nssv3564641
Samples
Known GenesEMR1, EMR4P, FLJ25758, MBD3L2, MBD3L3, MBD3L4, MBD3L5, ZNF557
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063107
Frequency
Sample Size29084
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer