A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433466



Internal ID22491336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134629056..134640670hg38UCSC Ensembl
chr7:134313808..134325422hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3811615
hg1911615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922361
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433466
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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