A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633658



Internal ID21581963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33864546..33864546hg38UCSC Ensembl
chr6:33832323..33832323hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151658
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633658
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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