A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585042



Internal ID21533586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38043670..38043773hg38UCSC Ensembl
chr10:38332598..38332701hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070191
SamplesNA18534
Known GenesZNF33A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585042
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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