A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406737



Internal ID21064290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107563014..107577978hg38UCSC Ensembl
chr5:106898715..106913679hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3814965
hg1914965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124233
Samples
Known GenesEFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406737
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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