A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590851



Internal ID16378260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84595035..84729928hg38UCSC Ensembl
Innerchr3:84644186..84779079hg19UCSC Ensembl
Innerchr3:84726876..84861769hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38134894
hg19134894
hg18134894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv967325
Samples
Known GenesLINC00971
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590851
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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