A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569081



Internal ID21517434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107073197..107073250hg38UCSC Ensembl
chr6:107394401..107394454hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154297
SamplesHG02818
Known GenesBEND3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569081
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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