A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104611



Internal ID21509195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35580619..35580619hg38UCSC Ensembl
chr19:36071521..36071521hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381044
hg191044
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653963
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104611
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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