A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551494



Internal ID20924628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26529021..26529860hg38UCSC Ensembl
chr22:26924987..26925826hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38840
hg19840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073170
Samples
Known GenesTPST2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551494
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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