A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584664



Internal ID21533207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77036199..77036544hg38UCSC Ensembl
chr18:74748155..74748500hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17102116
SamplesHG02818
Known GenesMBP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584664
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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