A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509666



Internal ID18807947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40834692..40987414hg38UCSC Ensembl
Innerchr11:40856242..41008964hg19UCSC Ensembl
Innerchr11:40812818..40965540hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38152723
hg19152723
hg18152723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039904
Supporting Variants
Samples
Known GenesLRRC4C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3509666
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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