A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933745



Internal ID22709060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67932309..67932404hg38UCSC Ensembl
chr17:65928425..65928520hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378558
Samples
Known GenesBPTF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933745
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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