A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661411



Internal ID18959692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55141086..55153962hg38UCSC Ensembl
Innerchr7:55208779..55221655hg19UCSC Ensembl
Innerchr7:55176273..55189149hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3812877
hg1912877
hg1812877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030862
Supporting Variants
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)nssv3661411
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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