A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067102



Internal ID21462053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91040256..91040379hg38UCSC Ensembl
chr1:91505813..91505936hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570244
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067102
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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