A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036701



Internal ID18779232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49825038..50810134hg38UCSC Ensembl
Innerchr11:49846590..50769305hg19UCSC Ensembl
Innerchr11:49803166..50725881hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38985097
hg19922716
hg18922716
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1128n100
Supporting Variantsnssv3505378
Samples
Known GenesLOC441601, LOC646813, OR4C12, OR4C13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036701
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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