A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352541



Internal ID22265126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69409867..69409918hg38UCSC Ensembl
chr10:71169623..71169674hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222424
Supporting Variants
SamplesNA19238
Known GenesTACR2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352541
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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