A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058136



Internal ID18800667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48561514..48594891hg38UCSC Ensembl
Innerchr19:49064771..49098148hg19UCSC Ensembl
Innerchr19:53756583..53789960hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3833378
hg1933378
hg1833378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3574968
Samples
Known GenesSULT2B1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058136
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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