A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097019



Internal ID21470721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69920216..69920216hg38UCSC Ensembl
chr15:70212555..70212555hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654161
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097019
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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