A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705532



Internal ID15095498
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528853
Supporting Variants
Samples
Known GenesEGFR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705532
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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