A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060808



Internal ID21457466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152196259..152196338hg38UCSC Ensembl
chr1:152168735..152168814hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576456
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060808
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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