A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018658



Internal ID19107875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55139754..55151056hg38UCSC Ensembl
Innerchr7:55207447..55218749hg19UCSC Ensembl
Innerchr7:55174941..55186243hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3811303
hg1911303
hg1811303
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6357n100
Supporting Variantsnssv3661358, nssv3661347, nssv3661362, nssv3661349, nssv3661356, nssv3661357, nssv3661354, nssv3661352, nssv3661359, nssv3661365, nssv3661351, nssv3661361, nssv3661364, nssv3661370, nssv3661366, nssv3661360, nssv3661369, nssv3661348, nssv3661353, nssv3661368, nssv3661355, nssv3661350, nssv3661363, nssv3661367
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)nsv1018658
Frequency
Sample Size11257
Observed Gain11
Observed Loss13
Observed Complex0
Frequencyn/a


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