A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228068



Internal ID22370367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43975838..43976012hg38UCSC Ensembl
chr17:42053206..42053380hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3574n152
Supporting Variantsnssv14378503, nssv14384123, nssv14386792
SamplesNA19238, NA19239, NA19240
Known GenesPYY
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228068
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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