A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640213



Internal ID21588518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75927807..75927807hg38UCSC Ensembl
chr6:76637524..76637524hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg384784
hg194784
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158938
SamplesNA18939
Known GenesIMPG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640213
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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