A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3503138



Internal ID18801419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85419499..85509729hg38UCSC Ensembl
Innerchr11:85130543..85220773hg19UCSC Ensembl
Innerchr11:84808191..84898421hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3890231
hg1990231
hg1890231
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035905
Supporting Variants
Samples
Known GenesDLG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3503138
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