A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446034



Internal ID22112213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149311642..149311808hg38UCSC Ensembl
chr6:149632778..149632944hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763864
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446034
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