A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047823



Internal ID19137042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97107874..97226033hg38UCSC Ensembl
Innerchr11:96978874..97097033hg19UCSC Ensembl
Innerchr11:96484084..96602243hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38118160
hg19118160
hg18118160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1258n100
Supporting Variantsnssv3514331
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)nsv1047823
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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