A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035113



Internal ID19124332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55139754..55151489hg38UCSC Ensembl
Innerchr7:55207447..55219182hg19UCSC Ensembl
Innerchr7:55174941..55186676hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3811736
hg1911736
hg1811736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6356n100
Supporting Variantsnssv3661374, nssv3661372, nssv3661376, nssv3661377, nssv3661375, nssv3661378, nssv3661373
Samples
Known GenesEGFR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035113
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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