A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541109



Internal ID20914394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40390839..40393703hg38UCSC Ensembl
chr22:40786843..40789707hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg382865
hg192865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073823
Samples
Known GenesSGSM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541109
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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