A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935589



Internal ID22710933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75866413..75889112hg38UCSC Ensembl
chr17:73862494..73885193hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3822700
hg1922700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379029
Samples
Known GenesTRIM47, TRIM65
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935589
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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