A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022907



Internal ID18765441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55138237..55150982hg38UCSC Ensembl
Innerchr7:55205930..55218675hg19UCSC Ensembl
Innerchr7:55173424..55186169hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3812746
hg1912746
hg1812746
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6356n100
Supporting Variantsnssv3661329
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)nsv1022907
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