A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156116



Internal ID21454952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132752690..132753331hg38UCSC Ensembl
chr8:133764936..133765577hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580689
Supporting Variants
SamplesHG02011
Known GenesTMEM71
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156116
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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