A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024599



Internal ID21933942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28318809..28321562hg38UCSC Ensembl
chr17:26645835..26648588hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382754
hg192754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633683
Samples
Known GenesTMEM97
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024599
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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