A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436679



Internal ID22494549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47141822..47159939hg38UCSC Ensembl
chr8:48053445..48071562hg19UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3818118
hg1918118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917509
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436679
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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