A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642636



Internal ID21590941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5895230..5895230hg38UCSC Ensembl
chr6:5895463..5895463hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145083
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642636
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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