A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536259



Internal ID20909612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30192401..30193500hg38UCSC Ensembl
chr22:30588390..30589489hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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