A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661379



Internal ID18959660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55139754..55153474hg38UCSC Ensembl
Innerchr7:55207447..55221167hg19UCSC Ensembl
Innerchr7:55174941..55188661hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3813721
hg1913721
hg1813721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018862
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)nssv3661379
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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