A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637936



Internal ID21586241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17249723..17249723hg38UCSC Ensembl
chr6:17249954..17249954hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152052
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637936
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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