A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368375



Internal ID22594044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94286773..94287456hg38UCSC Ensembl
chr10:96046530..96047213hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921698
Supporting Variants
Samples
Known GenesPLCE1, PLCE1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368375
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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