A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626347



Internal ID21574652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137696802..137696802hg38UCSC Ensembl
chr6:138017939..138017939hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38589
hg19589
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142403
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626347
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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