A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528853



Internal ID15109460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:54997426..55020722hg38UCSC Ensembl
Innerchr7:55065119..55088415hg19UCSC Ensembl
Innerchr7:55032613..55055909hg18UCSC Ensembl
Innerchr7:54839328..54862624hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3823297
hg1923297
hg1823297
hg1723297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705532
Samples
Known GenesEGFR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528853
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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