A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590137



Internal ID21538706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125710948..125717559hg38UCSC Ensembl
chr10:127399517..127406128hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386612
hg196612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067648
SamplesHG00732
Known GenesFLJ37035
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590137
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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