A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437755



Internal ID22495625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143808341..143808422hg38UCSC Ensembl
chr8:144890511..144890592hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914114
Supporting Variants
Samples
Known GenesSCRIB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437755
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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