A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033353



Internal ID21942696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44718294..44718376hg38UCSC Ensembl
chr17:42795662..42795744hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626554
Samples
Known GenesDBF4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033353
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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