A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047004



Internal ID19136223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84617415..84653551hg38UCSC Ensembl
Innerchr11:84328458..84364594hg19UCSC Ensembl
Innerchr11:84006106..84042242hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3836137
hg1936137
hg1836137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3509756, nssv3522085
Samples
Known GenesDLG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047004
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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