A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7089n54



Internal ID22774984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:140651597..140714156hg38UCSC Ensembl
chr2:141409166..141471725hg19UCSC Ensembl
chr2:141125636..141188195hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3862560
hg1962560
hg1862560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv583195, nsv583194
Samples
Known GenesLRP1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7089n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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