A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567165



Internal ID21759208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20836598..20836735hg38UCSC Ensembl
chr7:20876217..20876354hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008294
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567165
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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