A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594139



Internal ID21542734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:194513..205777hg38UCSC Ensembl
chr19:194513..205777hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3811265
hg1911265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103410
SamplesHG03125
Known GenesLINC01002
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594139
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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