A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827886



Internal ID15775156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:50704161..50733474hg38UCSC Ensembl
Innerchr14:51170879..51200192hg19UCSC Ensembl
Innerchr14:50240629..50269942hg18UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3829314
hg1929314
hg1829314
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564840
Supporting Variants
Samples
Known GenesNIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv827886
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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