A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537704



Internal ID20911039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32175246..32231403hg38UCSC Ensembl
chr22:32571233..32627390hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3856158
hg1956158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073769
Samples
Known GenesRFPL2, SLC5A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537704
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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