A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575627



Internal ID21524057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77887912..77887962hg38UCSC Ensembl
chr1:78353597..78353647hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066443
SamplesHG03371
Known GenesNEXN-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575627
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