A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16992103



Internal ID62183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:470181..471330hg38UCSC Ensembl
chr7:509818..510967hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381150
hg191150
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419267
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16992103
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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