A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047211



Internal ID19136430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44653884..44764023hg38UCSC Ensembl
Innerchr14:45123087..45233226hg19UCSC Ensembl
Innerchr14:44192837..44302976hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38110140
hg19110140
hg18110140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1901n100
Supporting Variantsnssv3530330, nssv3530331
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047211
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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