A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225377



Internal ID22368523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53561347..53563021hg38UCSC Ensembl
chr17:51638708..51640382hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381675
hg191675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14378845
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225377
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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