A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032857



Internal ID19122079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55138889..55151056hg38UCSC Ensembl
Innerchr7:55206582..55218749hg19UCSC Ensembl
Innerchr7:55174076..55186243hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3812168
hg1912168
hg1812168
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6357n100
Supporting Variantsnssv3661336, nssv3661333, nssv3661334, nssv3661335, nssv3661332, nssv3661337
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)nsv1032857
Frequency
Sample Size11257
Observed Gain5
Observed Loss1
Observed Complex0
Frequencyn/a


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