A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437233



Internal ID22495103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27851153..27851505hg38UCSC Ensembl
chr7:27890772..27891124hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920578
Supporting Variants
Samples
Known GenesJAZF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437233
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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