A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090855



Internal ID21479460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32928771..32928942hg38UCSC Ensembl
chr17:31255789..31255960hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595827
Supporting Variants
SamplesHG03486
Known GenesTMEM98
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090855
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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