A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545908



Internal ID15986631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26509300..26661535hg38UCSC Ensembl
Innerchr1:26835791..26988026hg19UCSC Ensembl
Innerchr1:26708378..26860613hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38152236
hg19152236
hg18152236
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712043
Samples
Known GenesMIR1976, RPS6KA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545908
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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