A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587314



Internal ID21535874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42195668..42196066hg38UCSC Ensembl
chr17:40347686..40348084hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089835
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587314
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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