A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143382



Internal ID21488824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:56639287..56639370hg38UCSC Ensembl
chr7:56706980..56707063hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567450
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143382
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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