A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437236



Internal ID22103414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81511247..81511301hg38UCSC Ensembl
chr9:84126162..84126216hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767414
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437236
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