A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526704



Internal ID15453997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:19749252..19749508hg38UCSC Ensembl
Innerchr11:19770798..19771054hg19UCSC Ensembl
Innerchr11:19727374..19727630hg18UCSC Ensembl
Innerchr11:19727374..19727630hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38257
hg19257
hg18257
hg17257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703043
Samples
Known GenesNAV2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526704
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