A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627439



Internal ID21575744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41357594..41357594hg38UCSC Ensembl
chr6:41325332..41325332hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156296
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627439
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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