A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657919



Internal ID21606224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101099062..101099062hg38UCSC Ensembl
chr13:101751413..101751413hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088094
SamplesHG03125
Known GenesNALCN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657919
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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