A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105558



Internal ID21473341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53657519..53657519hg38UCSC Ensembl
chr19:54160773..54160773hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645236
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105558
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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