A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360346



Internal ID21017899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25851906..25945523hg38UCSC Ensembl
chr3:25893397..25987014hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3893618
hg1993618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101145
Samples
Known GenesLINC00692
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360346
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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