A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640393



Internal ID21588698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110772889..110772889hg38UCSC Ensembl
chr6:111094092..111094092hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148780
SamplesHG00512
Known GenesCDK19
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640393
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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