A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922810



Internal ID22698035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29470789..29477133hg38UCSC Ensembl
chr8:29328306..29334650hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg386345
hg196345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436992
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922810
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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