A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573567



Internal ID21521973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169963840..169963889hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151188
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573567
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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