A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104751



Internal ID21458413
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 StatusS
Merged Variantsnsv5646719
Supporting Variants
SamplesHG02587
Known GenesTSHZ3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104751
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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