A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575674



Internal ID21524105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74543279..74543336hg38UCSC Ensembl
chr6:75252995..75253052hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144018
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575674
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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