A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17164738



Internal ID21471155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115347133..115347133hg38UCSC Ensembl
chr19:34570028..34570028hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605701
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17164738
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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