A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064684



Internal ID18807215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15311319..16062011hg38UCSC Ensembl
Innerchr19:15422130..16172821hg19UCSC Ensembl
Innerchr19:15283130..16033821hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38750693
hg19750692
hg18750692
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723292
Samples
Known GenesAKAP8, AKAP8L, CYP4F11, CYP4F12, CYP4F2, CYP4F22, CYP4F24P, CYP4F3, CYP4F8, LINC00661, LINC00905, MIR1470, OR10H1, OR10H2, OR10H3, OR10H4, OR10H5, PGLYRP2, RASAL3, UCA1, WIZ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064684
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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