A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051841



Internal ID19141060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:23975608..24019798hg38UCSC Ensembl
Innerchr14:24444817..24489007hg19UCSC Ensembl
Innerchr14:23514657..23558847hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3844191
hg1944191
hg1844191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1842n100
Supporting Variantsnssv3712201, nssv3712204, nssv3712205, nssv3712202, nssv3528417, nssv3528416, nssv3712203
Samples
Known GenesDHRS4L1, DHRS4L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051841
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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