A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068497



Internal ID21463026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103974652..103974735hg38UCSC Ensembl
chr10:105734410..105734493hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589464
Supporting Variants
SamplesHG03009
Known GenesSLK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068497
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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