A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220537



Internal ID22365203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18741447..18741597hg38UCSC Ensembl
chr10:19030376..19030526hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv824n152
Supporting Variantsnssv14333138, nssv14333139
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220537
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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