A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053725



Internal ID19142944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37383718..37427833hg38UCSC Ensembl
Innerchr11:37405268..37449383hg19UCSC Ensembl
Innerchr11:37361844..37405959hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3844116
hg1944116
hg1844116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1098n100
Supporting Variantsnssv3520176
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)nsv1053725
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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