A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595827



Internal ID21544434
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 StatusM
Merged Variants
Supporting Variantsnssv17090855
SamplesHG03486
Known GenesTMEM98
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595827
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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