A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198656



Internal ID22348354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28273202..28273818hg38UCSC Ensembl
chr6:28240979..28241595hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14327595
SamplesHG00733
Known GenesZSCAN26
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198656
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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