A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661341



Internal ID18959622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55138889..55153474hg38UCSC Ensembl
Innerchr7:55206582..55221167hg19UCSC Ensembl
Innerchr7:55174076..55188661hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3814586
hg1914586
hg1814586
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028514
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)nssv3661341
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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