A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626554



Internal ID21818601
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 StatusS
Merged Variantsnsv6033353
Supporting Variants
Samples
Known GenesDBF4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626554
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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