A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088036



Internal ID21433750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70376497..70376497hg38UCSC Ensembl
chr15:70668836..70668836hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656025
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088036
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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