A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095135



Internal ID21461771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56062857..56062857hg38UCSC Ensembl
chr15:56355055..56355055hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646800
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095135
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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