A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908298



Internal ID22683508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5237424..5356654hg38UCSC Ensembl
chr10:5279387..5398617hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38119231
hg19119231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357453
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908298
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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