A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657191



Internal ID21605496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43559097..43559097hg38UCSC Ensembl
chr19:44063249..44063249hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105245
SamplesNA20847
Known GenesXRCC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657191
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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