A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485019



Internal ID262416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100087711..100087894hg38UCSC Ensembl
chr9:102849993..102850176hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025552
Samples
Known GenesERP44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485019
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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