A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911012



Internal ID22686224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68799747..68802978hg38UCSC Ensembl
chr10:70559504..70562735hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383232
hg193232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358942
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911012
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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