A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913947



Internal ID22689163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34945365..34982884hg38UCSC Ensembl
chr8:34802883..34840402hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3837520
hg1937520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436320
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913947
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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