A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223436



Internal ID22367204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104108292..104108348hg38UCSC Ensembl
chr10:105868050..105868106hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1039n152
Supporting Variantsnssv14353675, nssv14353674
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223436
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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