A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545420



Internal ID15986143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:11747913..11751226hg38UCSC Ensembl
Innerchr1:11807970..11811283hg19UCSC Ensembl
Innerchr1:11730557..11733870hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg383314
hg193314
hg183314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv709939
Samples
Known GenesAGTRAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545420
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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