A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549176



Internal ID20922344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49240628..49241686hg38UCSC Ensembl
chr20:47857165..47858223hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg381059
hg191059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068984
Samples
Known GenesDDX27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549176
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