A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446806



Internal ID22112983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67613288..67613356hg38UCSC Ensembl
chr13:68187420..68187488hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757842
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446806
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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