A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103638



Internal ID21493635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16031803..16031803hg38UCSC Ensembl
chr19:16142613..16142613hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661310
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103638
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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