A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920064



Internal ID22695287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87259643..87264650hg38UCSC Ensembl
chr9:89874558..89879565hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg385008
hg195008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431613
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920064
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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