A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915655



Internal ID22690873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133366588..133366771hg38UCSC Ensembl
chr10:135180092..135180275hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358355
Samples
Known GenesECHS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915655
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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