A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv799951



Internal ID16093907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:85129154..85172430hg38UCSC Ensembl
Innerchr12:85522932..85566208hg19UCSC Ensembl
Innerchr12:84047063..84090339hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3843277
hg1943277
hg1843277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559657
Supporting Variants
Samples
Known GenesLRRIQ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv799951
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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