A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6356n100



Internal ID22792443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55136415..55153962hg38UCSC Ensembl
chr7:55204108..55221655hg19UCSC Ensembl
chr7:55171602..55189149hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3817548
hg1917548
hg1817548
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031055, nsv1022735, nsv1026867, nsv1022907, nsv1024580, nsv1025115, nsv1034313, nsv1028509, nsv1035113
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)dgv6356n100
Frequency
Sample Size11257
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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