A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222577



Internal ID22366612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37509155..37509266hg38UCSC Ensembl
chr17:35869261..35869368hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38112
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14380180, nssv14386224
SamplesHG00512, HG00732
Known GenesDUSP14
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222577
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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