A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545266



Internal ID15985989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6464441..6470375hg38UCSC Ensembl
Innerchr1:6524501..6530435hg19UCSC Ensembl
Innerchr1:6447088..6453022hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg385935
hg195935
hg185935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv709211
Samples
Known GenesPLEKHG5, TNFRSF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545266
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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