A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018872



Internal ID19108089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55138889..55153962hg38UCSC Ensembl
Innerchr7:55206582..55221655hg19UCSC Ensembl
Innerchr7:55174076..55189149hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3815074
hg1915074
hg1815074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6358n100
Supporting Variantsnssv3661346
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)nsv1018872
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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