A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16992863



Internal ID62706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20988194..20991838hg38UCSC Ensembl
chr7:21027813..21031457hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg383645
hg193645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468504
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16992863
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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