A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909611



Internal ID22684821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38507873..38507938hg38UCSC Ensembl
chr8:38365391..38365456hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909611
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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