A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015132



Internal ID19104349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17268389..17293502hg38UCSC Ensembl
Innerchr1:17594884..17619997hg19UCSC Ensembl
Innerchr1:17467471..17492584hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3825114
hg1925114
hg1825114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv129n100
Supporting Variantsnssv3700292, nssv3471294, nssv3482567, nssv3700291, nssv3466433, nssv3473402, nssv3700288, nssv3700290, nssv3469634, nssv3463421, nssv3476433, nssv3700289, nssv3468949, nssv3700293
Samples
Known GenesPADI3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015132
Frequency
Sample Size11257
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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