A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565951



Internal ID21514269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104774081..104774392hg38UCSC Ensembl
chr6:105221956..105222267hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144724
SamplesNA19238
Known GenesHACE1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565951
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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