A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567690



Internal ID21759733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134629057..134640667hg38UCSC Ensembl
chr7:134313809..134325419hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3811611
hg1911611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567690
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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