A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523373



Internal ID15450666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18361364..18379984hg38UCSC Ensembl
Innerchr11:18382911..18401531hg19UCSC Ensembl
Innerchr11:18339487..18358107hg18UCSC Ensembl
Innerchr11:18339487..18358107hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3818621
hg1918621
hg1818621
hg1718621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699122
Samples
Known GenesGTF2H1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523373
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