A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636953



Internal ID21585258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125644262..125644262hg38UCSC Ensembl
chr10:127332831..127332831hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38862
hg19862
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067646
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636953
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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