A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518900



Internal ID15446193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:173209352..173221723hg38UCSC Ensembl
Innerchr4:174130503..174142874hg19UCSC Ensembl
Innerchr4:174367078..174379449hg18UCSC Ensembl
Innerchr4:174505233..174517604hg17UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3812372
hg1912372
hg1812372
hg1712372
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696358
Samples
Known GenesGALNT7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518900
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