A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538645



Internal ID20911959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30376001..30378100hg38UCSC Ensembl
chr22:30771990..30774089hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073675
Samples
Known GenesCCDC157, KIAA1656
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538645
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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