A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544937



Internal ID15985660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1028484..1032208hg38UCSC Ensembl
Innerchr1:963864..967588hg19UCSC Ensembl
Innerchr1:953727..957451hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg383725
hg193725
hg183725
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv708455
Samples
Known GenesAGRN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544937
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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