A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601490



Internal ID21550137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49069970..49070286hg38UCSC Ensembl
chr10:50278015..50278331hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070616
SamplesHG00512
Known GenesVSTM4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601490
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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