A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333753



Internal ID20866933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3867072..3871398hg38UCSC Ensembl
chr1:3783636..3787962hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg384327
hg194327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061264
Samples
Known GenesDFFB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333753
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