A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642467



Internal ID21590772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73563830..73563830hg38UCSC Ensembl
chr6:74273553..74273553hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141186
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642467
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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