A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590425



Internal ID21538993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39902656..39903046hg38UCSC Ensembl
chr17:38058909..38059299hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082660
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590425
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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