A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920746



Internal ID22695969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29654204..29654408hg38UCSC Ensembl
chr10:29943133..29943337hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363431
Samples
Known GenesSVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920746
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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