A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525721



Internal ID15106328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42897688..42901990hg38UCSC Ensembl
Innerchr4:42899705..42904007hg19UCSC Ensembl
Innerchr4:42594462..42598764hg18UCSC Ensembl
Innerchr4:42740633..42744935hg17UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg384303
hg194303
hg184303
hg174303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701884
Samples
Known GenesGRXCR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525721
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