A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545439



Internal ID15986162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12182702..12186118hg38UCSC Ensembl
Innerchr1:12242759..12246175hg19UCSC Ensembl
Innerchr1:12165346..12168762hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg383417
hg193417
hg183417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv112n54
Supporting Variantsnssv710019, nssv710018
Samples
Known GenesTNFRSF1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545439
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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