A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631236



Internal ID21579541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41738241..41738241hg38UCSC Ensembl
chr6:41705979..41705979hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158945
SamplesHG03065
Known GenesPGC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631236
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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