A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044041



Internal ID18786572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71588129..71827945hg38UCSC Ensembl
Innerchr11:71299175..71538991hg19UCSC Ensembl
Innerchr11:70976823..71216639hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38239817
hg19239817
hg18239817
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1222n100
Supporting Variantsnssv3710648
Samples
Known GenesALG1L9P, FAM86C1, ZNF705E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044041
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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