A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931678



Internal ID22706965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75925125..77416814hg38UCSC Ensembl
chr14:76391468..77883157hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381491690
hg191491690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388976
Samples
Known GenesANGEL1, C14orf166B, ESRRB, GPATCH2L, GSTZ1, IFT43, IRF2BPL, KIAA1737, LOC100506603, MIR1260A, NGB, NOXRED1, POMT2, RNU6-19P, RNU6-31P, SAMD15, TGFB3, TMED8, TMEM63C, TTLL5, VASH1, ZDHHC22
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931678
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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