A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564770



Internal ID16352179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47120191..47191173hg38UCSC Ensembl
Innerchr14:47589394..47660376hg19UCSC Ensembl
Innerchr14:46659144..46730126hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3870983
hg1970983
hg1870983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3703n54
Supporting Variantsnssv827703, nssv827702
Samples
Known GenesMDGA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564770
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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