A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368234



Internal ID21025787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87151901..87156800hg38UCSC Ensembl
chr3:87201051..87205950hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104157
Samples
Known GenesLINC00506
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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