A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120904



Internal ID21471238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40898219..40898551hg38UCSC Ensembl
chr22:41294223..41294555hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601365
Supporting Variants
SamplesHG03125
Known GenesXPNPEP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120904
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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