A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932456



Internal ID22707754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56895613..56902151hg38UCSC Ensembl
chr17:54972974..54979512hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg386539
hg196539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370697
Samples
Known GenesTRIM25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932456
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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