A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408227



Internal ID21065780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117440501..117447300hg38UCSC Ensembl
chr5:116776197..116782996hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125766
Samples
Known GenesLINC00992
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408227
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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