A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593787



Internal ID21542378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91439463..91455952hg38UCSC Ensembl
chr10:93199220..93215709hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3816490
hg1916490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072264
SamplesHG03732
Known GenesHECTD2, LOC100188947
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593787
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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