A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613131



Internal ID21561436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16537888..16537888hg38UCSC Ensembl
chr3:16579395..16579395hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133091
SamplesHG00171
Known GenesLINC00690
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613131
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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