A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856565



Internal ID22631500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18195579..18200965hg38UCSC Ensembl
chrUn_gl000212:24331..29717hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg385387
hg195387
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456891, nssv17451239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856565
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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