A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369527



Internal ID21027080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97073143..97201065hg38UCSC Ensembl
chr3:96791987..96919909hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38127923
hg19127923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104838
Samples
Known GenesEPHA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369527
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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