A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441644



Internal ID22107825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37589398..37589680hg38UCSC Ensembl
chr21:38961700..38961982hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763386
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441644
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