A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993227



Internal ID62937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23034242..23041621hg38UCSC Ensembl
chr7:23073861..23081240hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg387380
hg197380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462470
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993227
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001928


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