A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105588



Internal ID21505438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44357939..44358161hg38UCSC Ensembl
chr19:44862091..44862313hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596066
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105588
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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