A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087348



Internal ID21451337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34295097..34297996hg38UCSC Ensembl
chr17:32622116..32625015hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587565
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087348
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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