A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027152



Internal ID85818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123113604..123113671hg38UCSC Ensembl
chr9:125875883..125875950hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488205
Supporting Variants
Samples
Known GenesMIR600HG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027152
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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