A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439985



Internal ID22497855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:114925949..114936149hg38UCSC Ensembl
chr8:115938178..115948378hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3810201
hg1910201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926284
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439985
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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