A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592603



Internal ID21541186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11514163..11514240hg38UCSC Ensembl
chr10:11556162..11556239hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066715
SamplesHG00731
Known GenesUSP6NL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592603
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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