A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567054



Internal ID21515385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38144172..38144225hg38UCSC Ensembl
chr6:38111948..38112001hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145355
SamplesNA19239
Known GenesZFAND3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567054
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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