A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571800



Internal ID21520182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51535905..51535966hg38UCSC Ensembl
chr5:50831739..50831800hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121129
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571800
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