A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197111



Internal ID22347028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186462156..186462427hg38UCSC Ensembl
chr3:186179945..186180216hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14310916, nssv14310915
SamplesHG00512, HG00514
Known GenesLOC253573
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197111
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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