A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564132



Internal ID16351541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27568292..27626617hg38UCSC Ensembl
Innerchr14:28037498..28095823hg19UCSC Ensembl
Innerchr14:27107338..27165663hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3858326
hg1958326
hg1858326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3593n54
Supporting Variantsnssv825072
Samples
Known GenesLINC00645
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564132
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