A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601146



Internal ID21549790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60185480..60185602hg38UCSC Ensembl
chr17:58262841..58262963hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096096
SamplesHG00096
Known GenesUSP32
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601146
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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