A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893395



Internal ID22668455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114067327..114068272hg38UCSC Ensembl
chr6:114388491..114389436hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38946
hg19946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421923
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893395
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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