A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630515



Internal ID21578820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107138510..107138510hg38UCSC Ensembl
chr6:107459714..107459714hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139930
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630515
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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