A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585033



Internal ID21533577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63015467..63015871hg38UCSC Ensembl
chr10:64775227..64775631hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070463
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585033
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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