A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221486



Internal ID22365859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140035969..140036056hg38UCSC Ensembl
chr7:139735769..139735856hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8777n152
Supporting Variantsnssv14337018
SamplesHG00512
Known GenesPARP12
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221486
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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