A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054456



Internal ID18796987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:104488196..104934524hg38UCSC Ensembl
Innerchr11:104358924..104805251hg19UCSC Ensembl
Innerchr11:103864134..104310461hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38446329
hg19446328
hg18446328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710738
Samples
Known GenesCASP12, LOC643733
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054456
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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