A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087544



Internal ID21488063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60184681..60185342hg38UCSC Ensembl
chr17:58262042..58262703hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590750
Supporting Variants
SamplesNA18534
Known GenesUSP32
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087544
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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