A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3507067



Internal ID18805348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62356434..62404820hg38UCSC Ensembl
Innerchr11:62123906..62172292hg19UCSC Ensembl
Innerchr11:61880482..61928868hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3848387
hg1948387
hg1848387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039105
Supporting Variants
Samples
Known GenesASRGL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3507067
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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