A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630153



Internal ID21578458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132600859..132600859hg38UCSC Ensembl
chr6:132921998..132921998hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142060, nssv17154714
SamplesHG03486, HG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630153
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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