A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941465



Internal ID21361534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95079876..95079969hg38UCSC Ensembl
chr8:96092104..96092197hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15199612
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3941465
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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