A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635556



Internal ID21583861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70845656..70845656hg38UCSC Ensembl
chr10:72605413..72605413hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071804
SamplesHG00512
Known GenesSGPL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635556
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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