A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6357n100



Internal ID22792444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55138889..55151210hg38UCSC Ensembl
chr7:55206582..55218903hg19UCSC Ensembl
chr7:55174076..55186397hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3812322
hg1912322
hg1812322
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033998, nsv1018658, nsv1016909, nsv1032857
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)dgv6357n100
Frequency
Sample Size11257
Observed Gain18
Observed Loss24
Observed Complex0
Frequencyn/a


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