A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154099



Internal ID21425104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30246697..30246773hg38UCSC Ensembl
chr8:30104213..30104289hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578825
Supporting Variants
SamplesHG00731
Known GenesMIR548O2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154099
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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