A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406611



Internal ID21064164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139029301..139037100hg38UCSC Ensembl
chr5:138364990..138372789hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125379
Samples
Known GenesSIL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406611
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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