A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594791



Internal ID21543391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70918600..70918661hg38UCSC Ensembl
chr10:72678357..72678418hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071805
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594791
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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