A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438189



Internal ID22496059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126408812..126416658hg38UCSC Ensembl
chr8:127421057..127428903hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg387847
hg197847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923001
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438189
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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