A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851034



Internal ID22625969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18183657..18188228hg38UCSC Ensembl
chrUn_gl000212:12409..16980hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384572
hg194572
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458905, nssv17457865, nssv17467057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851034
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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