A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525222



Internal ID22394598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69110387..69110724hg38UCSC Ensembl
chr3:69159538..69159875hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5999n152
Supporting Variantsnssv14307457, nssv14307455, nssv14307456
SamplesHG00512, HG00732, NA19240
Known GenesLMOD3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525222
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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