A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597345



Internal ID21545957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49964164..49964287hg38UCSC Ensembl
chr10:51723924..51724047hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070793
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597345
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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