A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369876



Internal ID21027429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14134101..14140000hg38UCSC Ensembl
chr4:14135725..14141624hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108171
Samples
Known GenesLINC01085
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369876
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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