A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017702



Internal ID19106919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55140462..55151056hg38UCSC Ensembl
Innerchr7:55208155..55218749hg19UCSC Ensembl
Innerchr7:55175649..55186243hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3810595
hg1910595
hg1810595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6358n100
Supporting Variantsnssv3661395
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)nsv1017702
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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