A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571750



Internal ID16359159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28598169..28609431hg38UCSC Ensembl
Innerchr16:28609490..28620752hg19UCSC Ensembl
Innerchr16:28516991..28528253hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3811263
hg1911263
hg1811263
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4975n54
Supporting Variantsnssv855289, nssv855293, nssv855291, nssv855288, nssv855287, nssv855290, nssv855286, nssv855292
Samples
Known GenesSULT1A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571750
Frequency
Sample Size17421
Observed Gain5
Observed Loss3
Observed Complex0
Frequencyn/a


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