A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628406



Internal ID21576711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118304985..118304985hg38UCSC Ensembl
chr6:118626148..118626148hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157640
SamplesHG00732
Known GenesSLC35F1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628406
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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