A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv142n21



Internal ID22766334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100051488..100066865hg38UCSC Ensembl
chr14:100517825..100533202hg19UCSC Ensembl
chr14:99587578..99602955hg18UCSC Ensembl
chr14:99587578..99602955hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3815378
hg1915378
hg1815378
hg1715378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv518128, nsv527606
Samples
Known GenesEVL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv142n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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