A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7091n54



Internal ID22774986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:141502023..141537473hg38UCSC Ensembl
chr2:142259592..142295042hg19UCSC Ensembl
chr2:141976062..142011512hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3835451
hg1935451
hg1835451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv583211, nsv583210
SamplesHGDP00090
Known GenesLRP1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7091n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer