A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15199569



Internal ID21338365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41626350..41626454hg38UCSC Ensembl
chr8:41483869..41483973hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938594
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15199569
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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