A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545238



Internal ID15985961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6248510..6257923hg38UCSC Ensembl
Innerchr1:6308570..6317983hg19UCSC Ensembl
Innerchr1:6231157..6240570hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg389414
hg199414
hg189414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv709152
Samples
Known GenesGPR153
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545238
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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