A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035910



Internal ID19125129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81725388..81847748hg38UCSC Ensembl
Innerchr11:81436430..81558790hg19UCSC Ensembl
Innerchr11:81114078..81236438hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38122361
hg19122361
hg18122361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1242n100
Supporting Variantsnssv3503150
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)nsv1035910
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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