A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573793



Internal ID21522201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107680063..107680177hg38UCSC Ensembl
chr7:107320508..107320622hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140590
SamplesHG02011
Known GenesSLC26A4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573793
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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