A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071747



Internal ID21457705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87839787..87839836hg38UCSC Ensembl
chr10:89599544..89599593hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592172
Supporting Variants
SamplesHG02587
Known GenesCFL1P1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071747
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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