A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16992335



Internal ID62351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2707438..2709591hg38UCSC Ensembl
chr7:2747072..2749225hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg382154
hg192154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458659
Supporting Variants
Samples
Known GenesAMZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16992335
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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