A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528931



Internal ID15109538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:4489997..4501034hg38UCSC Ensembl
Innerchr4:4491724..4502761hg19UCSC Ensembl
Innerchr4:4542625..4553662hg18UCSC Ensembl
Innerchr4:4609796..4620833hg17UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3811038
hg1911038
hg1811038
hg1711038
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705621
Samples
Known GenesSTX18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528931
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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