A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601845



Internal ID20974916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109154801..109156500hg38UCSC Ensembl
chr6:109476004..109477703hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137033
Samples
Known GenesCEP57L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601845
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