A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv855411



Internal ID16149367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28603413..28609990hg38UCSC Ensembl
Innerchr16:28614734..28621311hg19UCSC Ensembl
Innerchr16:28522235..28528812hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg386578
hg196578
hg186578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571771
Supporting Variants
Samples
Known GenesSULT1A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv855411
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