A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601019



Internal ID21549663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27942769..27943077hg38UCSC Ensembl
chr22:28338757..28339065hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138035
SamplesHG01596
Known GenesTTC28-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601019
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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