A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639782



Internal ID21588087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117924263..117924263hg38UCSC Ensembl
chr6:118245426..118245426hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157923
SamplesHG00731
Known GenesSLC35F1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639782
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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