A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162673



Internal ID21457268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81615656..81615728hg38UCSC Ensembl
chr9:84230571..84230643hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590600
Supporting Variants
SamplesHG02587
Known GenesTLE1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162673
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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