A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639799



Internal ID21588104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90661722..90661722hg38UCSC Ensembl
chr6:91371441..91371441hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153059
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639799
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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