A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043059



Internal ID19132278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48319210..48447768hg38UCSC Ensembl
Innerchr14:48788413..48916971hg19UCSC Ensembl
Innerchr14:47858163..47986721hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38128559
hg19128559
hg18128559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1918n100
Supporting Variantsnssv3713490
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)nsv1043059
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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