A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991500



Internal ID61743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3136286..3141552hg38UCSC Ensembl
chr7:3175920..3181186hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg385267
hg195267
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470408
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991500
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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