A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144504



Internal ID21465741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106319983..106320062hg38UCSC Ensembl
chr7:105960429..105960508hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574293
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144504
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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