A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138377



Internal ID21402985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28794677..28794677hg38UCSC Ensembl
chr22:29190665..29190665hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg382934
hg192934
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671515
Supporting Variants
SamplesHG00171
Known GenesXBP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138377
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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