A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591038



Internal ID21539610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38058499..38058604hg38UCSC Ensembl
chr10:38347427..38347532hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070192
SamplesHG03065
Known GenesZNF33A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591038
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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