A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590407



Internal ID21538975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7745632..7745769hg38UCSC Ensembl
chr19:7810518..7810655hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106879
SamplesHG02492
Known GenesCD209
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590407
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