A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000062



Internal ID67621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97100492..97121237hg38UCSC Ensembl
chr7:96729804..96750549hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3820746
hg1920746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484951
Supporting Variants
Samples
Known GenesACN9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000062
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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