A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035946



Internal ID19125165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80256492..80270277hg38UCSC Ensembl
Innerchr11:79967536..79981321hg19UCSC Ensembl
Innerchr11:79645184..79658969hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3813786
hg1913786
hg1813786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1236n100
Supporting Variantsnssv3514379, nssv3517031, nssv3511308
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)nsv1035946
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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