A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089117



Internal ID21458095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39351440..39351440hg38UCSC Ensembl
chr13:39925577..39925577hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656335
Supporting Variants
SamplesHG02587
Known GenesLHFP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089117
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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