A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409247



Internal ID21066800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133215147..133216527hg38UCSC Ensembl
chr5:132550839..132552219hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg381381
hg191381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127168
Samples
Known GenesFSTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409247
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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