A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085695



Internal ID21456186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21027255..21027334hg38UCSC Ensembl
chr17:20930568..20930647hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603034
Supporting Variants
SamplesHG02492
Known GenesUSP22
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085695
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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