A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104644



Internal ID21493801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3762006..3762006hg38UCSC Ensembl
chr19:3762004..3762004hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662610
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104644
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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