A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv825142



Internal ID16119098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:30912145..30956231hg38UCSC Ensembl
Innerchr14:31381351..31425437hg19UCSC Ensembl
Innerchr14:30451102..30495188hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3844087
hg1944087
hg1844087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564177
Supporting Variants
Samples
Known GenesSTRN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv825142
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