A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016909



Internal ID19106126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55140383..55151056hg38UCSC Ensembl
Innerchr7:55208076..55218749hg19UCSC Ensembl
Innerchr7:55175570..55186243hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3810674
hg1910674
hg1810674
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6357n100
Supporting Variantsnssv3661390, nssv3661389, nssv3661388, nssv3661387
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)nsv1016909
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer