A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025115



Internal ID18767647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55138237..55151028hg38UCSC Ensembl
Innerchr7:55205930..55218721hg19UCSC Ensembl
Innerchr7:55173424..55186215hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3812792
hg1912792
hg1812792
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6356n100
Supporting Variantsnssv3661330
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)nsv1025115
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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