A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566057



Internal ID21514376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160601521..160603270hg38UCSC Ensembl
chr6:161022553..161024302hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381750
hg191750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157283
SamplesHG03125
Known GenesLPA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566057
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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