A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214537



Internal ID22361162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36195447..36198356hg38UCSC Ensembl
chr10:36484375..36487284hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg382910
hg192910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14340701
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214537
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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