A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15199095



Internal ID21337891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102640589..102640661hg38UCSC Ensembl
chr8:103652817..103652889hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3950561
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15199095
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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