A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374988



Internal ID21032541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87569761..87570685hg38UCSC Ensembl
chr3:87618911..87619835hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg38925
hg19925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104225
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374988
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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