A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051536



Internal ID19140755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3400993..3591901hg38UCSC Ensembl
Innerchr11:3422223..3613131hg19UCSC Ensembl
Innerchr11:3378799..3569707hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38190909
hg19190909
hg18190909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1018n100
Supporting Variantsnssv3520473
Samples
Known GenesLOC650368
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051536
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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