A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541915



Internal ID20915183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26238294..26245165hg38UCSC Ensembl
chr22:26634260..26641131hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg386872
hg196872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073158
Samples
Known GenesSEZ6L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541915
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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