A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571772



Internal ID16359181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28603480..28609431hg38UCSC Ensembl
Innerchr16:28614801..28620752hg19UCSC Ensembl
Innerchr16:28522302..28528253hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg385952
hg195952
hg185952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4981n54
Supporting Variantsnssv855412, nssv855413, nssv855414, nssv855415
Samples
Known GenesSULT1A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571772
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