A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526748



Internal ID15454041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7520075..7521782hg38UCSC Ensembl
Innerchr4:7521802..7523509hg19UCSC Ensembl
Innerchr4:7572702..7574409hg18UCSC Ensembl
Innerchr4:7639873..7641580hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381708
hg191708
hg181708
hg171708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703094
Samples
Known GenesSORCS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526748
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