A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661325



Internal ID18959606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55110510..55151489hg38UCSC Ensembl
Innerchr7:55178203..55219182hg19UCSC Ensembl
Innerchr7:55145697..55186676hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3840980
hg1940980
hg1840980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031740
Supporting Variants
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)nssv3661325
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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