A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635554



Internal ID21583859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160603284..160603284hg38UCSC Ensembl
chr6:161024316..161024316hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381405
hg191405
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141842
SamplesHG03125
Known GenesLPA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635554
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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