A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096213



Internal ID21500568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49652608..49652608hg38UCSC Ensembl
chr15:49944805..49944805hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656985
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096213
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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