A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925468



Internal ID22700695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17135353..17140586hg38UCSC Ensembl
chr8:16992862..16998095hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg385234
hg195234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429822
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925468
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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