A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv915981



Internal ID16209937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:108282832..108298972hg38UCSC Ensembl
Innerchr2:108899288..108915428hg19UCSC Ensembl
Innerchr2:108265720..108281860hg18UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg3816141
hg1916141
hg1816141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582640
Supporting Variants
Samples
Known GenesSULT1C2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv915981
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