A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041610



Internal ID19130829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80256508..80271129hg38UCSC Ensembl
Innerchr11:79967552..79982173hg19UCSC Ensembl
Innerchr11:79645200..79659821hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3814622
hg1914622
hg1814622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1236n100
Supporting Variantsnssv3513252
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041610
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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