A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944324



Internal ID21364393
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15199128
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944324
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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