A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593108



Internal ID21541693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9273966..9274058hg38UCSC Ensembl
chr10:9315929..9316021hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071548
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593108
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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