A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14328553



Internal ID22282164
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224741
Supporting Variants
SamplesNA19239
Known GenesIL15RA
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14328553
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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