A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862798



Internal ID22637733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18220601..18233135hg38UCSC Ensembl
chrUn_gl000212:49353..61887hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3812535
hg1912535
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456175, nssv17450201, nssv17453670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862798
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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