A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910502



Internal ID22685713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30739117..30739932hg38UCSC Ensembl
chr10:31028046..31028861hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361859
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910502
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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