A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148951



Internal ID15876256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38489763..38569077hg38UCSC Ensembl
Innerchr14:38958967..39038281hg19UCSC Ensembl
Innerchr14:38028718..38108032hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3879315
hg1979315
hg1879315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564413
Supporting Variants
SamplesHGDP00810
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148951
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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