A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032917



Internal ID19122139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55141086..55153474hg38UCSC Ensembl
Innerchr7:55208779..55221167hg19UCSC Ensembl
Innerchr7:55176273..55188661hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3812389
hg1912389
hg1812389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6358n100
Supporting Variantsnssv3661406, nssv3661405, nssv3661407
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)nsv1032917
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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