A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142952



Internal ID21511471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106143155..106143213hg38UCSC Ensembl
chr8:107155383..107155441hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582265
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142952
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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