A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514331



Internal ID18812612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97107874..97226033hg38UCSC Ensembl
Innerchr11:96978874..97097033hg19UCSC Ensembl
Innerchr11:96484084..96602243hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38118160
hg19118160
hg18118160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047823
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3514331
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