A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661371



Internal ID18959652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55139754..55151210hg38UCSC Ensembl
Innerchr7:55207447..55218903hg19UCSC Ensembl
Innerchr7:55174941..55186397hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3811457
hg1911457
hg1811457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028457
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)nssv3661371
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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