A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586977



Internal ID21535535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68258079..68258135hg38UCSC Ensembl
chr17:66254220..66254276hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088855
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586977
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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