A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907771



Internal ID22682981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94093924..94094239hg38UCSC Ensembl
chr10:95853681..95853996hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369332
Samples
Known GenesPLCE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907771
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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