A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545611



Internal ID15986334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15683836..15684641hg38UCSC Ensembl
Innerchr1:16010331..16011136hg19UCSC Ensembl
Innerchr1:15882918..15883723hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38806
hg19806
hg18806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv149n54
Supporting Variantsnssv710535, nssv710534
Samples
Known GenesPLEKHM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545611
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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