A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200892



Internal ID22350281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27278922..27279525hg38UCSC Ensembl
chr6:27246701..27247304hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14326904
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200892
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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