A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545921



Internal ID15986644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28781383..28839626hg38UCSC Ensembl
Innerchr1:29107895..29166138hg19UCSC Ensembl
Innerchr1:28980482..29038725hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3858244
hg1958244
hg1858244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173805
Samples1782681216_A
Known GenesOPRD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545921
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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