A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587565



Internal ID21536123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34295097..34297996hg38UCSC Ensembl
chr17:32622116..32625015hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087348
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587565
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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