A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646719



Internal ID21595024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31337390..31337390hg38UCSC Ensembl
chr19:31828296..31828296hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104751
SamplesHG02587
Known GenesTSHZ3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646719
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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