A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592064



Internal ID21540644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75186188..75193073hg38UCSC Ensembl
chr17:73182283..73189168hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg386886
hg196886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095612
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592064
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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