A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465774



Internal ID22523663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20119370..20121250hg38UCSC Ensembl
chr10:20408299..20410179hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381881
hg191881
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854169
Supporting Variants
Samples
Known GenesPLXDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465774
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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