A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035635



Internal ID18778166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:796542..911980hg38UCSC Ensembl
Innerchr11:796542..911980hg19UCSC Ensembl
Innerchr11:786542..901980hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38115439
hg19115439
hg18115439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1013n100
Supporting Variantsnssv3503025, nssv3516501, nssv3516801
Samples
Known GenesCD151, CHID1, EFCAB4A, PIDD, PNPLA2, POLR2L, RPLP2, SLC25A22, SNORA52, TSPAN4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035635
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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