A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592986



Internal ID21541571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15979643..15979692hg38UCSC Ensembl
chr17:15882957..15883006hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080697
SamplesHG00171
Known GenesZSWIM7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592986
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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