A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377095



Internal ID21034648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10223801..10225800hg38UCSC Ensembl
chr5:10223913..10225912hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122064
Samples
Known GenesFAM173B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377095
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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