A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577838



Internal ID21526296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169765858..169766001hg38UCSC Ensembl
chr6:170165954..170166097hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147557
SamplesHG00732
Known GenesERMARD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577838
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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