A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590743



Internal ID21539313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56223986..56224035hg38UCSC Ensembl
chr19:56735355..56735404hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106326
SamplesHG02818
Known GenesZSCAN5A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590743
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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