A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444199



Internal ID22502069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:114082728..114087900hg38UCSC Ensembl
chr8:115094957..115100129hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg385173
hg195173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921463
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444199
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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