A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564588



Internal ID22433318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42216385..42216385hg38UCSC Ensembl
chr6:42184123..42184123hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14326454
SamplesHG00513
Known GenesMRPS10
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564588
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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