A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564640



Internal ID22433370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28325553..28325553hg38UCSC Ensembl
chr6:28293330..28293330hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14327597, nssv14327596
SamplesNA19239, NA19240
Known GenesZSCAN31
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564640
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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