A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550476



Internal ID20923617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28129168..28141411hg38UCSC Ensembl
chr22:28525156..28537399hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3812244
hg1912244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073242
Samples
Known GenesTTC28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550476
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer