A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17443814



Internal ID22501684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22407123..22414088hg38UCSC Ensembl
chr7:22446742..22453707hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg386966
hg196966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918502
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17443814
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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