A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407927



Internal ID21065480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107396610..107397189hg38UCSC Ensembl
chr5:106732311..106732890hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124222
Samples
Known GenesEFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407927
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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