A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035905



Internal ID19125124
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 StatusM
Merged Variants
Supporting Variantsnssv3503138
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)nsv1035905
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