A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497636



Internal ID20870844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93916065..93921868hg38UCSC Ensembl
chr14:94382411..94388214hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg385804
hg195804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022908
Samples
Known GenesFAM181A, FAM181A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497636
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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