A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413380



Internal ID21070933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117449922..117452799hg38UCSC Ensembl
chr5:116785618..116788495hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg382878
hg192878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125768
Samples
Known GenesLINC00992
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413380
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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