A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350593



Internal ID22576262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:19994269..19994269hg38UCSC Ensembl
chr10:20283198..20283198hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947686
Supporting Variants
Samples
Known GenesPLXDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350593
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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