A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2765n54



Internal ID22770660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:85129154..85209753hg38UCSC Ensembl
chr12:85522932..85603531hg19UCSC Ensembl
chr12:84047063..84127662hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3880600
hg1980600
hg1880600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv559660, nsv559658
Samples
Known GenesLRRIQ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2765n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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