A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578969



Internal ID21527444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10786378..10786727hg38UCSC Ensembl
chr6:10786611..10786960hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144739
SamplesHG02818
Known GenesMAK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578969
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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