A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15199128



Internal ID21337924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:129647236..129647286hg38UCSC Ensembl
chr8:130659482..130659532hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3944324
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15199128
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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