A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152034



Internal ID21468249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152371875..152371924hg38UCSC Ensembl
chr6:152693010..152693059hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569379
Supporting Variants
SamplesHG03125
Known GenesSYNE1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152034
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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