A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433487



Internal ID22491357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125056229..125091575hg38UCSC Ensembl
chr8:126068471..126103817hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3835347
hg1935347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921918
Supporting Variants
Samples
Known GenesKIAA0196
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433487
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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