A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640593



Internal ID21588898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42216385..42216385hg38UCSC Ensembl
chr6:42184123..42184123hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148605
SamplesHG01114
Known GenesMRPS10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640593
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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