A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033998



Internal ID19123220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55141086..55151210hg38UCSC Ensembl
Innerchr7:55208779..55218903hg19UCSC Ensembl
Innerchr7:55176273..55186397hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3810125
hg1910125
hg1810125
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6357n100
Supporting Variantsnssv3661403, nssv3661397, nssv3661401, nssv3661400, nssv3661399, nssv3661398, nssv3661402, nssv3661404
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)nsv1033998
Frequency
Sample Size11257
Observed Gain1
Observed Loss7
Observed Complex0
Frequencyn/a


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