A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526177



Internal ID15453470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:138208101..138234650hg38UCSC Ensembl
Innerchr4:139129255..139155804hg19UCSC Ensembl
Innerchr4:139348705..139375254hg18UCSC Ensembl
Innerchr4:139486860..139513409hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3826550
hg1926550
hg1826550
hg1726550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702438
Samples
Known GenesSLC7A11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526177
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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