A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224741



Internal ID22368079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5967284..5968018hg38UCSC Ensembl
chr10:6009247..6009981hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14328553
SamplesNA19239
Known GenesIL15RA
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224741
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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