A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142862



Internal ID21489496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:785223..785299hg38UCSC Ensembl
chr7:824860..824936hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572373
Supporting Variants
SamplesNA18939
Known GenesHEATR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142862
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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