A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918393



Internal ID22693614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100087711..100087886hg38UCSC Ensembl
chr9:102849993..102850168hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445961
Samples
Known GenesERP44
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918393
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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