A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681573



Internal ID15071539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128513182..128516011hg38UCSC Ensembl
Innerchr11:128383077..128385906hg19UCSC Ensembl
Innerchr11:127888287..127891116hg18UCSC Ensembl
Innerchr11:127888287..127891116hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382830
hg192830
hg182830
hg172830
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517012
Supporting Variants
Samples
Known GenesETS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681573
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